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rs1807467

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1807467(G;T)
Make rs1807467(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position18918380
GenePRODH
is asnp
is mentioned by
dbSNPrs1807467
ebirs1807467
HLIrs1807467
Exacrs1807467
Varsomers1807467
Maprs1807467
PheGenIrs1807467
hapmaprs1807467
1000 genomesrs1807467
hgdprs1807467
ensemblrs1807467
gopubmedrs1807467
geneviewrs1807467
scholarrs1807467
googlers1807467
pharmgkbrs1807467
gwascentralrs1807467
openSNPrs1807467
23andMers1807467
23andMe allrs1807467
SNP Nexus

SNPshotrs1807467
SNPdbers1807467
MSV3drs1807467
GWAS Ctlgrs1807467
Max Magnitude0
OMIM606810
DescHYPERPROLINEMIA, TYPE I
Variant0005
Relatedalso
Neighborrs2870984
Distance34
Neighborrs3970559
Distance6
ClinVar
Risk rs1807467(T;T)
Alt rs1807467(T;T)
Reference rs1807467(G;G)
Significance Other
Disease Proline dehydrogenase deficiency Schizophrenia 4
Variation info
Gene PRODH
CLNDBN Proline dehydrogenase deficiency Schizophrenia 4
Reversed 1
HGVS NC_000022.10:g.18905893C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004220.6, RCV000004221.6,