Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.41 (G)

Chromosome 11:7008610 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs4468329, rs60892257

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2513 sample genotypes.

Variant displays