Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 17:39722873 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1164932, rs57255947

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2506 sample genotypes.

Variant displays