Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.23 (T)
Location

Chromosome 1:186640617 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.186640617C>T

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays