Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.20 (A)
Location

Chromosome 5:159391737 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59783909

HGVS name

5:g.159391737A>C

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_ImmunoChip

Variation displays