Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.49 (C)

Chromosome 11:69811925 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56825162

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2508 sample genotypes.

Variant displays