Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.28 (C)
Location

Chromosome X:48828708 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61535102, rs6520382

HGVS name

X:g.48828708T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays