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rs780882740

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780882740(C;T)
Make rs780882740(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136434050
GeneINPP5E
is asnp
is mentioned by
dbSNPrs780882740
ebirs780882740
HLIrs780882740
Exacrs780882740
Varsomers780882740
Maprs780882740
PheGenIrs780882740
hapmaprs780882740
1000 genomesrs780882740
hgdprs780882740
ensemblrs780882740
gopubmedrs780882740
geneviewrs780882740
scholarrs780882740
googlers780882740
pharmgkbrs780882740
gwascentralrs780882740
openSNPrs780882740
23andMers780882740
23andMe allrs780882740
SNP Nexus

SNPshotrs780882740
SNPdbers780882740
MSV3drs780882740
GWAS Ctlgrs780882740
Max Magnitude0
ClinVar
Risk rs780882740(T;T)
Alt rs780882740(T;T)
Reference rs780882740(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.139328502C>T
CLNSRC
CLNACC RCV000201735.1,