Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.15 (G)

Chromosome 6:39723717 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs113644178, rs58659339

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2509 sample genotypes.

Variant displays