Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 15:44583958 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs52789918

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 264 sample genotypes.

Variant displays