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 12:11802291 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.11802291C>G

Variation displays