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
Location

Chromosome X:71117448 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.71117448T>G

Variation displays