Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.13 (G)
Location

Chromosome 4:147558564 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.147558564C>G

Variation displays