Original source

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

G/T | Ancestral: T | Ambiguity code: K | MAF: 0.35 (T)

Chromosome 20:7938749 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2578 sample genotypes.

Variant displays