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rs16945894

From SNPedia

Orientationplus
Stabilizedplus
Make rs16945894(C;C)
Make rs16945894(C;T)
Make rs16945894(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position48146199
GeneABCC12
is asnp
is mentioned by
dbSNPrs16945894
ebirs16945894
HLIrs16945894
Exacrs16945894
Varsomers16945894
Maprs16945894
PheGenIrs16945894
hapmaprs16945894
1000 genomesrs16945894
hgdprs16945894
ensemblrs16945894
gopubmedrs16945894
geneviewrs16945894
scholarrs16945894
googlers16945894
pharmgkbrs16945894
gwascentralrs16945894
openSNPrs16945894
23andMers16945894
23andMe allrs16945894
SNP Nexus

SNPshotrs16945894
SNPdbers16945894
MSV3drs16945894
GWAS Ctlgrs16945894
Max Magnitude
? (C;C) (C;T) (T;T) 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-6
Odds Ratio NR NR