Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.12 (T)
Location

Chromosome 1:116908876 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59907887

HGVS name

1:g.116908876C>T

This variation has assays on 4 chips - click the plus to show

Variation displays