Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (C)
Location

Chromosome 10:23191641 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.23191641T>C

Variation displays