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rs10743430

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10743430(C;C)
Make rs10743430(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position21998639
is asnp
is mentioned by
dbSNPrs10743430
ebirs10743430
HLIrs10743430
Exacrs10743430
Varsomers10743430
Maprs10743430
PheGenIrs10743430
hapmaprs10743430
1000 genomesrs10743430
hgdprs10743430
ensemblrs10743430
gopubmedrs10743430
geneviewrs10743430
scholarrs10743430
googlers10743430
pharmgkbrs10743430
gwascentralrs10743430
openSNPrs10743430
23andMers10743430
23andMe allrs10743430
SNP Nexus

SNPshotrs10743430
SNPdbers10743430
MSV3drs10743430
GWAS Ctlgrs10743430
GMAF0.191
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21116278]
Trait
Title Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
Risk Allele
P-val 6E-7
Odds Ratio 0.2181 [NR] unit decrease (main effect)