Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome X:3604043 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.3604043C>A

About this variant

This variant overlaps 3 transcripts.

Variation displays