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rs372127610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372127610(A;A)
Make rs372127610(A;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position13222352
GeneMPDZ
is asnp
is mentioned by
dbSNPrs372127610
ebirs372127610
HLIrs372127610
Exacrs372127610
Varsomers372127610
Maprs372127610
PheGenIrs372127610
hapmaprs372127610
1000 genomesrs372127610
hgdprs372127610
ensemblrs372127610
gopubmedrs372127610
geneviewrs372127610
scholarrs372127610
googlers372127610
pharmgkbrs372127610
gwascentralrs372127610
openSNPrs372127610
23andMers372127610
23andMe allrs372127610
SNP Nexus

SNPshotrs372127610
SNPdbers372127610
MSV3drs372127610
GWAS Ctlgrs372127610
Max Magnitude0
ClinVar
Risk rs372127610(A;A)
Alt rs372127610(A;A)
Reference rs372127610(G;G)
Significance Pathogenic
Disease Hydrocephalus
Variation info
Gene MPDZ
CLNDBN Hydrocephalus, nonsyndromic, autosomal recessive 2
Reversed 0
HGVS NC_000009.11:g.13222351G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043475.3,