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rs10131300

From SNPedia

Orientationplus
Stabilizedplus
Make rs10131300(A;A)
Make rs10131300(A;C)
Make rs10131300(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position72472787
GeneRGS6
is asnp
is mentioned by
dbSNPrs10131300
ebirs10131300
HLIrs10131300
Exacrs10131300
Varsomers10131300
Maprs10131300
PheGenIrs10131300
hapmaprs10131300
1000 genomesrs10131300
hgdprs10131300
ensemblrs10131300
gopubmedrs10131300
geneviewrs10131300
scholarrs10131300
googlers10131300
pharmgkbrs10131300
gwascentralrs10131300
openSNPrs10131300
23andMers10131300
23andMe allrs10131300
SNP Nexus

SNPshotrs10131300
SNPdbers10131300
MSV3drs10131300
GWAS Ctlgrs10131300
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 5E-6
Odds Ratio NR NR