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rs2247208

From SNPedia

Orientationplus
Stabilizedplus
Make rs2247208(A;A)
Make rs2247208(A;G)
Make rs2247208(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position204908524
GeneNFASC
is asnp
is mentioned by
dbSNPrs2247208
ebirs2247208
HLIrs2247208
Exacrs2247208
Varsomers2247208
Maprs2247208
PheGenIrs2247208
hapmaprs2247208
1000 genomesrs2247208
hgdprs2247208
ensemblrs2247208
gopubmedrs2247208
geneviewrs2247208
scholarrs2247208
googlers2247208
pharmgkbrs2247208
gwascentralrs2247208
openSNPrs2247208
23andMers2247208
23andMe allrs2247208
SNP Nexus

SNPshotrs2247208
SNPdbers2247208
MSV3drs2247208
GWAS Ctlgrs2247208
Max Magnitude
? (A;A) (A;G) (G;G) 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 8E-6
Odds Ratio NR NR