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rs746867724

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746867724(A;A)
Make rs746867724(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136431090
GeneINPP5E
is asnp
is mentioned by
dbSNPrs746867724
ebirs746867724
HLIrs746867724
Exacrs746867724
Varsomers746867724
Maprs746867724
PheGenIrs746867724
hapmaprs746867724
1000 genomesrs746867724
hgdprs746867724
ensemblrs746867724
gopubmedrs746867724
geneviewrs746867724
scholarrs746867724
googlers746867724
pharmgkbrs746867724
gwascentralrs746867724
openSNPrs746867724
23andMers746867724
23andMe allrs746867724
SNP Nexus

SNPshotrs746867724
SNPdbers746867724
MSV3drs746867724
GWAS Ctlgrs746867724
Max Magnitude0
ClinVar
Risk rs746867724(A;A)
Alt rs746867724(A;A)
Reference rs746867724(G;G)
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.139325542G>A
CLNSRC
CLNACC RCV000201636.1,