Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome 4:74604379 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.74604379A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays