Rs2306677

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Orientationminus
Geno Mag Summary
(C;C) 0
Make rs2306677(C;T)
Make rs2306677(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position26483453
GeneITPR2
is asnp
is mentioned by
dbSNPrs2306677
Exacrs2306677
PheGenIrs2306677
nextbiors2306677
hapmaprs2306677
1000 genomesrs2306677
hgdprs2306677
ensemblrs2306677
gopubmedrs2306677
geneviewrs2306677
scholarrs2306677
googlers2306677
pharmgkbrs2306677
gwascentralrs2306677
openSNPrs2306677
23andMers2306677
23andMe allrs2306677
SNP Nexus

SNPshotrs2306677
SNPdbers2306677
MSV3drs2306677
GMAF0.1901
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs2306677
PubMedID [PMID 17827064]
Condition Amyotrophic lateral sclerosis
Gene ITPR2
Risk Allele
pValue 3.00E-006
OR 1.58
95% CI 1.30-1.91



[PMID 19193627OA-icon.png] A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.


GET Evidence
rs2306677
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.773438
summary



[PMID 22795786] No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population