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rs74315508

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs74315508(C;T)
Make rs74315508(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position20242778
GeneGNRH1, RTN4R
is asnp
is mentioned by
dbSNPrs74315508
ebirs74315508
HLIrs74315508
Exacrs74315508
Varsomers74315508
Maprs74315508
PheGenIrs74315508
hapmaprs74315508
1000 genomesrs74315508
hgdprs74315508
ensemblrs74315508
gopubmedrs74315508
geneviewrs74315508
scholarrs74315508
googlers74315508
pharmgkbrs74315508
gwascentralrs74315508
openSNPrs74315508
23andMers74315508
23andMe allrs74315508
SNP Nexus

SNPshotrs74315508
SNPdbers74315508
MSV3drs74315508
GWAS Ctlgrs74315508
GMAF0.003214
Max Magnitude0
OMIM605566
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315508(T;T)
Alt rs74315508(T;T)
Reference rs74315508(C;C)
Significance Other
Disease Schizophrenia
Variation info
Gene RTN4R
CLNDBN Schizophrenia, susceptibility to
Reversed 1
HGVS NC_000022.10:g.20230301G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005158.3,