Original source

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

Alleles
C/A | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 4:3504958 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.3504958C>A

Variation displays