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

rs863225202

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225202(C;C)
Make rs863225202(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136432986
GeneINPP5E
is asnp
is mentioned by
dbSNPrs863225202
ebirs863225202
HLIrs863225202
Exacrs863225202
Varsomers863225202
Maprs863225202
PheGenIrs863225202
hapmaprs863225202
1000 genomesrs863225202
hgdprs863225202
ensemblrs863225202
gopubmedrs863225202
geneviewrs863225202
scholarrs863225202
googlers863225202
pharmgkbrs863225202
gwascentralrs863225202
openSNPrs863225202
23andMers863225202
23andMe allrs863225202
SNP Nexus

SNPshotrs863225202
SNPdbers863225202
MSV3drs863225202
GWAS Ctlgrs863225202
Max Magnitude0
ClinVar
Risk rs863225202(C;C)
Alt rs863225202(C;C)
Reference rs863225202(T;T)
Significance Pathogenic
Disease Familial aplasia of the vermis
Variation info
Gene INPP5E
CLNDBN Familial aplasia of the vermis
Reversed 1
HGVS NC_000009.11:g.139327438A>G
CLNSRC
CLNACC RCV000201740.1,