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rs17057640

From SNPedia

Orientationplus
Stabilizedplus
Make rs17057640(C;C)
Make rs17057640(C;T)
Make rs17057640(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position129698209
GeneARHGAP18
is asnp
is mentioned by
dbSNPrs17057640
ebirs17057640
HLIrs17057640
Exacrs17057640
Varsomers17057640
Maprs17057640
PheGenIrs17057640
hapmaprs17057640
1000 genomesrs17057640
hgdprs17057640
ensemblrs17057640
gopubmedrs17057640
geneviewrs17057640
scholarrs17057640
googlers17057640
pharmgkbrs17057640
gwascentralrs17057640
openSNPrs17057640
23andMers17057640
23andMe allrs17057640
SNP Nexus

SNPshotrs17057640
SNPdbers17057640
MSV3drs17057640
GWAS Ctlgrs17057640
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24684796OA-icon.png]
Trait Cognitive function
Title Heritability and genetic association analysis of cognition in the Diabetes Heart Study.
Risk Allele C
P-val 5E-6
Odds Ratio 3.01 [1.73-4.28] unit decrease