Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.32 (C)
Location

Chromosome X:120426285 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

X:g.120426285T>C

This variation has assays on 8 chips - click the plus to show

Variation displays