Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224242(-;C)
Make rs863224242(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position46355524
GeneTRMU
is asnp
is mentioned by
dbSNPrs863224242
ClinGenrs863224242
ebirs863224242
HLIrs863224242
Exacrs863224242
Varsomers863224242
Maprs863224242
PheGenIrs863224242
hapmaprs863224242
1000 genomesrs863224242
hgdprs863224242
ensemblrs863224242
gopubmedrs863224242
geneviewrs863224242
scholarrs863224242
googlers863224242
pharmgkbrs863224242
gwascentralrs863224242
openSNPrs863224242
23andMers863224242
23andMe allrs863224242
SNP Nexus

SNPshotrs863224242
SNPdbers863224242
MSV3drs863224242
GWAS Ctlgrs863224242
Max Magnitude0
ClinVar
Risk rs863224242(C;C)
Alt rs863224242(C;C)
Reference Rs863224242(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TRMU
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.46751421dupC
CLNSRC
CLNACC RCV000197202.1,