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rs863225197

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225197(A;G)
Make rs863225197(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136430395
GeneINPP5E
is asnp
is mentioned by
dbSNPrs863225197
ebirs863225197
HLIrs863225197
Exacrs863225197
Varsomers863225197
Maprs863225197
PheGenIrs863225197
hapmaprs863225197
1000 genomesrs863225197
hgdprs863225197
ensemblrs863225197
gopubmedrs863225197
geneviewrs863225197
scholarrs863225197
googlers863225197
pharmgkbrs863225197
gwascentralrs863225197
openSNPrs863225197
23andMers863225197
23andMe allrs863225197
SNP Nexus

SNPshotrs863225197
SNPdbers863225197
MSV3drs863225197
GWAS Ctlgrs863225197
Max Magnitude0
ClinVar
Risk rs863225197(G;G)
Alt rs863225197(G;G)
Reference Rs863225197(A;A)
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.139324847T>C
CLNSRC
CLNACC RCV000201622.1,