Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 22:40345158 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.40345158T>G

Variation displays