Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.01 (A)
Location

Chromosome 19:44051163 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Variation displays