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: 0.01 (A)
Location

Chromosome 10:71962953 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.71962953C>A

Variation displays