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rs74315509

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs74315509(A;A)
Make rs74315509(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position20242546
GeneGNRH1, RTN4R
is asnp
is mentioned by
dbSNPrs74315509
ebirs74315509
HLIrs74315509
Exacrs74315509
Varsomers74315509
Maprs74315509
PheGenIrs74315509
hapmaprs74315509
1000 genomesrs74315509
hgdprs74315509
ensemblrs74315509
gopubmedrs74315509
geneviewrs74315509
scholarrs74315509
googlers74315509
pharmgkbrs74315509
gwascentralrs74315509
openSNPrs74315509
23andMers74315509
23andMe allrs74315509
SNP Nexus

SNPshotrs74315509
SNPdbers74315509
MSV3drs74315509
GWAS Ctlgrs74315509
Max Magnitude0
OMIM605566
Desc
Variant0002
Relatedalso
ClinVar
Risk rs74315509(A;A)
Alt rs74315509(A;A)
Reference rs74315509(G;G)
Significance Other
Disease Schizophrenia
Variation info
Gene RTN4R
CLNDBN Schizophrenia, susceptibility to
Reversed 1
HGVS NC_000022.10:g.20230069C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005159.3,