Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.06 (G)
Location

Chromosome X:2934197 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.2934197A>G

Variation displays