Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 2:118849894 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117016850

HGVS name

2:g.118849894C>A

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_Human1M-duo

Variation displays