Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.39 (T)

Chromosome 11:8089993 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57969751

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, has 2779 sample genotypes and is mentioned in 5 citations.

Variant displays