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rs863225198

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225198(C;T)
Make rs863225198(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136433250
GeneINPP5E
is asnp
is mentioned by
dbSNPrs863225198
ebirs863225198
HLIrs863225198
Exacrs863225198
Varsomers863225198
Maprs863225198
PheGenIrs863225198
hapmaprs863225198
1000 genomesrs863225198
hgdprs863225198
ensemblrs863225198
gopubmedrs863225198
geneviewrs863225198
scholarrs863225198
googlers863225198
pharmgkbrs863225198
gwascentralrs863225198
openSNPrs863225198
23andMers863225198
23andMe allrs863225198
SNP Nexus

SNPshotrs863225198
SNPdbers863225198
MSV3drs863225198
GWAS Ctlgrs863225198
Max Magnitude0
ClinVar
Risk rs863225198(T;T)
Alt rs863225198(T;T)
Reference rs863225198(C;C)
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.139327702G>A
CLNSRC
CLNACC RCV000201710.1,