Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 1:12209567 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

1:g.12209567C>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2552 individual genotypes.

Variation displays