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