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rs2870984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs2870984(A;A)
Make rs2870984(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position18918346
GenePRODH
is asnp
is mentioned by
dbSNPrs2870984
ebirs2870984
HLIrs2870984
Exacrs2870984
Varsomers2870984
Maprs2870984
PheGenIrs2870984
hapmaprs2870984
1000 genomesrs2870984
hgdprs2870984
ensemblrs2870984
gopubmedrs2870984
geneviewrs2870984
scholarrs2870984
googlers2870984
pharmgkbrs2870984
gwascentralrs2870984
openSNPrs2870984
23andMers2870984
23andMe allrs2870984
SNP Nexus

SNPshotrs2870984
SNPdbers2870984
MSV3drs2870984
GWAS Ctlgrs2870984
Max Magnitude0
OMIM606810
DescHYPERPROLINEMIA, TYPE I
Variant0009
Relatedalso
Neighborrs1807467
Distance34
Neighborrs2870983
Distance18


ClinVar
Risk rs2870984(A;A)
Alt rs2870984(A;A)
Reference rs2870984(G;G)
Significance Other
Disease Proline dehydrogenase deficiency Schizophrenia 4
Variation info
Gene PRODH
CLNDBN Proline dehydrogenase deficiency Schizophrenia 4
Reversed 0
HGVS NC_000022.10:g.18905859G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004227.7, RCV000004228.2,