rs_ID |
Location |
Functional Annotation |
rs12791871 |
Chr11:71164544(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7944926 |
Chr11:71165625(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1629220 |
Chr11:71174553(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1792226 |
Chr11:71176574(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1792229 |
Chr11:71179395(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs3794060 |
Chr11:71187679(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4945008 |
Chr11:71221248(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs11233747 |
Chr11:71171642(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2002064 |
Chr11:71163420(Fwd) |
downstream_gene_variant; intron_variant; upstream_gene_variant |
rs4423214 |
Chr11:71173254(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2040323 |
Chr11:71172783(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2276362 |
Chr11:71174452(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11600569 |
Chr11:71173747(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs2282620 |
Chr11:71183477(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2282621 |
Chr11:71183474(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4944062 |
Chr11:71187294(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7935125 |
Chr11:71184190(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1792234 |
Chr11:71182018(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4944957 |
Chr11:71168035(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1540127 |
Chr11:71179038(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12785878 |
Chr11:71167449(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1790343 |
Chr11:71177207(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4944959 |
Chr11:71168234(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4944958 |
Chr11:71168073(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7938885 |
Chr11:71170043(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs2276360 |
Chr11:71169547(Fwd) |
NMD_transcript_variant; downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
rs12790558 |
Chr11:71170905(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs12808368 |
Chr11:71170817(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |