Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.04 (G)
Location

Chromosome 22:41989257 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58577030, rs3171702

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2511 sample genotypes.

Variant displays