Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.45 (C)
Location

Chromosome 4:155512941 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR016061

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs28375882

HGVS name

4:g.155512941C>A

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni5

Variation displays