Original source

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

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

Chromosome 4:73740307 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR051279

Most severe consequence
Evidence status

HGVS name

4:g.73740307A>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays