Original source

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

Alleles
A/G/T | Ancestral: A | Ambiguity code: D
Location

Chromosome 15:63060915 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002641, CM941334 ; PhenCode FHC0623 (A/G), FHC0624 (A/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 86 HGVS names - click the plus to show

Variation displays