Have questions? Visit https://www.reddit.com/r/SNPedia

rs752300607

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752300607(C;T)
Make rs752300607(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position136430325
GeneINPP5E
is asnp
is mentioned by
dbSNPrs752300607
ebirs752300607
HLIrs752300607
Exacrs752300607
Varsomers752300607
Maprs752300607
PheGenIrs752300607
hapmaprs752300607
1000 genomesrs752300607
hgdprs752300607
ensemblrs752300607
gopubmedrs752300607
geneviewrs752300607
scholarrs752300607
googlers752300607
pharmgkbrs752300607
gwascentralrs752300607
openSNPrs752300607
23andMers752300607
23andMe allrs752300607
SNP Nexus

SNPshotrs752300607
SNPdbers752300607
MSV3drs752300607
GWAS Ctlgrs752300607
Max Magnitude0
ClinVar
Risk rs752300607(T;T)
Alt rs752300607(T;T)
Reference rs752300607(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.139324777C>T
CLNSRC
CLNACC RCV000201629.1,