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rs757222534

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs757222534(C;T)
Make rs757222534(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136431905
GeneINPP5E
is asnp
is mentioned by
dbSNPrs757222534
ebirs757222534
HLIrs757222534
Exacrs757222534
Varsomers757222534
Maprs757222534
PheGenIrs757222534
hapmaprs757222534
1000 genomesrs757222534
hgdprs757222534
ensemblrs757222534
gopubmedrs757222534
geneviewrs757222534
scholarrs757222534
googlers757222534
pharmgkbrs757222534
gwascentralrs757222534
openSNPrs757222534
23andMers757222534
23andMe allrs757222534
SNP Nexus

SNPshotrs757222534
SNPdbers757222534
MSV3drs757222534
GWAS Ctlgrs757222534
Max Magnitude0
ClinVar
Risk rs757222534(T;T)
Alt rs757222534(T;T)
Reference rs757222534(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.139326357C>A
CLNSRC
CLNACC RCV000201688.1,