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- Data Summary
SNP Report
Name | rs6697244 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr1:11838848(Fwd) | ||
Variant Alleles | G/T | ||
Ancestral Allele | G | ||
Functional Annotation | downstream_gene_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000484153) missense_variant(ENST00000433342; ENST00000312793) nc_transcript_variant(ENST00000376620) non_coding_exon_variant(ENST00000376620) upstream_gene_variant(ENST00000444493; ENST00000449278) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.