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 17:44034322 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.44034322C>A

Variation displays