Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.48 (C)
Location

Chromosome 2:9557243 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36217005

HGVS name

2:g.9557243A>C

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, has 3691 individual genotypes and is mentioned in 4 citations.

Variation displays