Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.50 (T)
Location

Chromosome 4:74606024 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR051279

Most severe consequence
Evidence status

HGVS name

4:g.74606024A>T

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays