Original source

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

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

Chromosome X:150563781 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.150563781C>G

Variation displays