Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.42 (G)

Chromosome 1:11021823 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 35 transcripts and has 2778 sample genotypes.

Variant displays