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rs4719220

From SNPedia

Orientationplus
Stabilizedplus
Make rs4719220(A;A)
Make rs4719220(A;G)
Make rs4719220(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position72215718
GeneCALN1
is asnp
is mentioned by
dbSNPrs4719220
ebirs4719220
HLIrs4719220
Exacrs4719220
Varsomers4719220
Maprs4719220
PheGenIrs4719220
hapmaprs4719220
1000 genomesrs4719220
hgdprs4719220
ensemblrs4719220
gopubmedrs4719220
geneviewrs4719220
scholarrs4719220
googlers4719220
pharmgkbrs4719220
gwascentralrs4719220
openSNPrs4719220
23andMers4719220
23andMe allrs4719220
SNP Nexus

SNPshotrs4719220
SNPdbers4719220
MSV3drs4719220
GWAS Ctlgrs4719220
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 4E-6
Odds Ratio NR NR