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 | MAF: 0.30 (C)
Location

Chromosome 15:63059641 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 26 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays