Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome X:151395439 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.151395439G>C

Variation displays