Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.07 (C)
Location

Chromosome 8:116618444 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58713577

HGVS name

8:g.116618444A>C

This variation has assays on 12 chips - click the plus to show

Variation displays