Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.01 (G)
Location

Chromosome X:48827398 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.48827398T>G

Variation displays