Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 4:3463521 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.3463521C>G

Variation displays