Original source

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

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

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

Most severe consequence
Missense variant
Evidence status

Clinical significance

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