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rs1801318

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1801318(A;G)
Make rs1801318(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position206141952
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs1801318
ebirs1801318
HLIrs1801318
Exacrs1801318
Varsomers1801318
Maprs1801318
PheGenIrs1801318
hapmaprs1801318
1000 genomesrs1801318
hgdprs1801318
ensemblrs1801318
gopubmedrs1801318
geneviewrs1801318
scholarrs1801318
googlers1801318
pharmgkbrs1801318
gwascentralrs1801318
openSNPrs1801318
23andMers1801318
23andMe allrs1801318
SNP Nexus

SNPshotrs1801318
SNPdbers1801318
MSV3drs1801318
GWAS Ctlgrs1801318
GMAF0.3269
Max Magnitude0

[PMID 24196945OA-icon.png] A Hypothesis Driven Association Study of 28 Nuclear-Encoded Mitochondrial Genes With Antipsychotic-Induced Weight Gain in Schizophrenia

? (A;A) (A;G) (G;G)
[PMID 16436204OA-icon.png] GPNN: power studies and applications of a neural network method for detecting gene-gene interactions in studies of human disease.


ClinVar
Risk rs1801318(G;G)
Alt rs1801318(G;G)
Reference rs1801318(A;A)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene NDUFS1
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.207006676T>C
CLNSRC ClinVar University of Chicago
CLNACC RCV000117709.2,