Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.02 (G)
Location

Chromosome 1:100314011 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.100314011C>G

Variation displays