Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.06 (T)
Location

Chromosome X:83508142 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.83508142G>T

Variation displays