Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.18 (A)
Location

Chromosome 2:119607470 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117016850

HGVS name

2:g.119607470C>A

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_1M-duo

Variation displays