Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome X:48683884 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.48683884T>C

Variation displays