Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.02 (C)
Location

Chromosome 4:174489876 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.174489876A>C

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays