Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome 1:169513832 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.169513832A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2504 individual genotypes.

Variation displays