Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 44 HGVS names - click the plus to show

Variation displays