Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.06 (G)
Location

Chromosome X:2934558 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.2934558C>G

Variation displays