Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.10 (C)
Location

Chromosome 1:110145631 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.110145631G>C

Variation displays