Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)
Location

Chromosome 1:12165317 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.12165317G>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts, has 2624 individual genotypes and is mentioned in 2 citations.

Variation displays