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rs13100616

From SNPedia

Orientationplus
Stabilizedplus
Make rs13100616(A;A)
Make rs13100616(A;G)
Make rs13100616(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position178681763
GeneKCNMB2
is asnp
is mentioned by
dbSNPrs13100616
ebirs13100616
HLIrs13100616
Exacrs13100616
Varsomers13100616
Maprs13100616
PheGenIrs13100616
hapmaprs13100616
1000 genomesrs13100616
hgdprs13100616
ensemblrs13100616
gopubmedrs13100616
geneviewrs13100616
scholarrs13100616
googlers13100616
pharmgkbrs13100616
gwascentralrs13100616
openSNPrs13100616
23andMers13100616
23andMe allrs13100616
SNP Nexus

SNPshotrs13100616
SNPdbers13100616
MSV3drs13100616
GWAS Ctlgrs13100616
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 9E-7
Odds Ratio NR NR