Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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