Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:70337298 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.70337298T>G

Variation displays