Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.36 (G)
Location

Chromosome X:43653054 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.43653054G>C

Variation displays