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rs746212325

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746212325(A;A)
Make rs746212325(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136434769
GeneINPP5E
is asnp
is mentioned by
dbSNPrs746212325
ebirs746212325
HLIrs746212325
Exacrs746212325
Varsomers746212325
Maprs746212325
PheGenIrs746212325
hapmaprs746212325
1000 genomesrs746212325
hgdprs746212325
ensemblrs746212325
gopubmedrs746212325
geneviewrs746212325
scholarrs746212325
googlers746212325
pharmgkbrs746212325
gwascentralrs746212325
openSNPrs746212325
23andMers746212325
23andMe allrs746212325
SNP Nexus

SNPshotrs746212325
SNPdbers746212325
MSV3drs746212325
GWAS Ctlgrs746212325
Max Magnitude0
ClinVar
Risk rs746212325(A,T;A,T)
Alt rs746212325(A,T;A,T)
Reference rs746212325(C;C)
Significance Pathogenic
Disease Familial aplasia of the vermis
Variation info
Gene INPP5E
CLNDBN Familial aplasia of the vermis
Reversed 0
HGVS NC_000009.11:g.139329221C>T
CLNSRC
CLNACC RCV000201762.1,