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rs797045095

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045095(C;T)
Make rs797045095(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position13123200
GeneMPDZ
is asnp
is mentioned by
dbSNPrs797045095
ebirs797045095
HLIrs797045095
Exacrs797045095
Varsomers797045095
Maprs797045095
PheGenIrs797045095
hapmaprs797045095
1000 genomesrs797045095
hgdprs797045095
ensemblrs797045095
gopubmedrs797045095
geneviewrs797045095
scholarrs797045095
googlers797045095
pharmgkbrs797045095
gwascentralrs797045095
openSNPrs797045095
23andMers797045095
23andMe allrs797045095
SNP Nexus

SNPshotrs797045095
SNPdbers797045095
MSV3drs797045095
GWAS Ctlgrs797045095
Max Magnitude0
ClinVar
Risk rs797045095(T;T)
Alt rs797045095(T;T)
Reference rs797045095(C;C)
Significance Probable-Pathogenic
Disease Hydrocephalus
Variation info
Gene MPDZ
CLNDBN Hydrocephalus, nonsyndromic, autosomal recessive 2
Reversed 1
HGVS NC_000009.11:g.13123199G>A
CLNSRC
CLNACC RCV000190604.1,