Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.36 (C)

Chromosome 11:44582341 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs16938007, rs57119829

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2582 sample genotypes.

Variant displays