Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 264 sample genotypes.

Variant displays