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rs2230774

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2230774(A;A)
Make rs2230774(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position11218994
GeneROCK2
is asnp
is mentioned by
dbSNPrs2230774
dbSNP (classic)rs2230774
ClinGenrs2230774
ebirs2230774
HLIrs2230774
Exacrs2230774
Gnomadrs2230774
Varsomers2230774
LitVarrs2230774
Maprs2230774
PheGenIrs2230774
Biobankrs2230774
1000 genomesrs2230774
hgdprs2230774
ensemblrs2230774
geneviewrs2230774
scholarrs2230774
googlers2230774
pharmgkbrs2230774
gwascentralrs2230774
openSNPrs2230774
23andMers2230774
SNPshotrs2230774
SNPdbers2230774
MSV3drs2230774
GWAS Ctlgrs2230774
GMAF0.4261
Max Magnitude0

[PMID 23326532OA-icon.png] Association analysis of polymorphisms in ROCK2 with cardiovascular disease in a Chinese population [PMID 18971541OA-icon.png] A major haplotype block at the rho-associated kinase 2 locus is associated with a lower risk of hypertension in a recessive manner: the HYPGENE study.


[PMID 22939913] Association between Rho-kinase (ROCK2) gene polymorphisms and Behcet's disease.

[PMID 26004609] Association of Rho/Rho-kinase gene polymorphisms and expressions with obesity-related metabolic syndrome [PMID 26818475] Polymorphisms and haplotype of ROCK2 associate with high altitude essential hypertension in native high altitude Ladakhi Indian population: a preliminary study.

ClinVar
Risk rs2230774(A;A) rs2230774(G;G)
Alt rs2230774(A;A) rs2230774(G;G)
Reference Rs2230774(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ROCK2
CLNDBN not specified
Reversed 1
HGVS NC_000002.11:g.11359120G>T
CLNSRC
CLNACC RCV000454422.1,