Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 22:40741300 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.40741300A>G

Variation displays