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rs633185

From SNPedia

Orientationminus
Stabilizedminus
Make rs633185(C;C)
Make rs633185(C;G)
Make rs633185(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position100722807
GeneARHGAP42
is asnp
is mentioned by
dbSNPrs633185
ebirs633185
HLIrs633185
Exacrs633185
Varsomers633185
Maprs633185
PheGenIrs633185
hapmaprs633185
1000 genomesrs633185
hgdprs633185
ensemblrs633185
gopubmedrs633185
geneviewrs633185
scholarrs633185
googlers633185
pharmgkbrs633185
gwascentralrs633185
openSNPrs633185
23andMers633185
23andMe allrs633185
SNP Nexus

SNPshotrs633185
SNPdbers633185
MSV3drs633185
GWAS Ctlgrs633185
GMAF0.348
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele G
P-val 2E-15
Odds Ratio 0.3280 [NR] mmHg decrease
GWAS snp
PMID [PMID 21909110OA-icon.png]
Trait
Title Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Risk Allele G
P-val 7E-10
Odds Ratio 0.3250 [0.22-0.43] mmHg decrease