SNP Report
Basic Info
Name |
rs6832751
dbSNP
Ensembl
|
Location |
Chr4:814080(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
G |
Functional Annotation |
intron_variant.
|
Consequence to Transcript |
intron_variant(ENST00000304062; ENST00000505203; ENST00000513195) |
No. of Studies |
1 (significant: 1; non-significant: 0; trend: 0) |
Source |
Literature-origin
|
SNP related studies (count: 1)
SNP related genes (count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.
Literature-origin SNPs (count: 0)
LD-proxies (count: 8)
rs_ID |
Functional Annotation |
r2[population] |
rs8093
|
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
0.808[GIH]
|
rs2127168
|
nc_transcript_variant; non_coding_exon_variant |
0.949[CEU]; 0.961[GIH]; 0.965[TSI]
|
rs10155282
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 0.961[GIH]; 1.0[JPT]; 1.0[MEX]; 1.0[TSI]
|
rs7663192
|
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
0.846[GIH]
|
rs7377207
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs1078139
|
downstream_gene_variant |
1.0[CEU]; 0.826[CHD]; 0.961[GIH]; 0.931[TSI]
|
rs4690332
|
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
0.846[GIH]
|
rs2306248
|
intron_variant; nc_transcript_variant; splice_region_variant |
0.809[GIH]
|