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rs797045707

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045707(A;A)
Make rs797045707(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position13221493
GeneMPDZ
is asnp
is mentioned by
dbSNPrs797045707
ebirs797045707
HLIrs797045707
Exacrs797045707
Varsomers797045707
Maprs797045707
PheGenIrs797045707
hapmaprs797045707
1000 genomesrs797045707
hgdprs797045707
ensemblrs797045707
gopubmedrs797045707
geneviewrs797045707
scholarrs797045707
googlers797045707
pharmgkbrs797045707
gwascentralrs797045707
openSNPrs797045707
23andMers797045707
23andMe allrs797045707
SNP Nexus

SNPshotrs797045707
SNPdbers797045707
MSV3drs797045707
GWAS Ctlgrs797045707
Max Magnitude0
ClinVar
Risk rs797045707(A;A)
Alt rs797045707(A;A)
Reference rs797045707(G;G)
Significance Pathogenic
Disease Hydrocephalus
Variation info
Gene MPDZ
CLNDBN Hydrocephalus, nonsyndromic, autosomal recessive 2
Reversed 1
HGVS NC_000009.11:g.13221492C>T
CLNSRC
CLNACC RCV000193063.1,