Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.26 (T)

Chromosome 7:151247038 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59423817

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 13 transcripts and has 3694 sample genotypes.

Variant displays