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rs754637179

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754637179(A;A)
Make rs754637179(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136434127
GeneINPP5E
is asnp
is mentioned by
dbSNPrs754637179
ebirs754637179
HLIrs754637179
Exacrs754637179
Varsomers754637179
Maprs754637179
PheGenIrs754637179
hapmaprs754637179
1000 genomesrs754637179
hgdprs754637179
ensemblrs754637179
gopubmedrs754637179
geneviewrs754637179
scholarrs754637179
googlers754637179
pharmgkbrs754637179
gwascentralrs754637179
openSNPrs754637179
23andMers754637179
23andMe allrs754637179
SNP Nexus

SNPshotrs754637179
SNPdbers754637179
MSV3drs754637179
GWAS Ctlgrs754637179
Max Magnitude0
ClinVar
Risk rs754637179(A;A)
Alt rs754637179(A;A)
Reference rs754637179(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.139328579G>A
CLNSRC
CLNACC RCV000201594.1,