Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.42 (A)
Location

Chromosome 17:18365454 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs6416873, rs10302254

HGVS name

17:g.18365454A>G

Variation displays