Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.04 (A)
Location

Chromosome X:3604103 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.3604103C>A

Variation displays