Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 16:88812323 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs837758, rs57492385

HGVS name

16:g.88812323A>G

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5

About this variant

This variant overlaps 18 transcripts and has 3772 individual genotypes.

Variation displays