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 15:63059591 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms
HGVS names

This variant has 44 HGVS names - Show

About this variant

This variant overlaps 32 transcripts, has 260 sample genotypes and is associated with 1 phenotype.

Variant displays