Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.16 (A)
Location

Chromosome 22:50584271 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs6010017

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2506 sample genotypes.

Variant displays