Original source

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

Alleles
G/C | Ambiguity code: S | MAF: 0.14 (G)
Location

Chromosome 17:65008950 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61461477

HGVS name

17:g.65008950G>C

Variation displays