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rs443198

From SNPedia

Orientationminus
Stabilizedminus
Make rs443198(C;C)
Make rs443198(C;T)
Make rs443198(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32222629
GeneNOTCH4
is asnp
is mentioned by
dbSNPrs443198
ebirs443198
HLIrs443198
Exacrs443198
Varsomers443198
Maprs443198
PheGenIrs443198
hapmaprs443198
1000 genomesrs443198
hgdprs443198
ensemblrs443198
gopubmedrs443198
geneviewrs443198
scholarrs443198
googlers443198
pharmgkbrs443198
gwascentralrs443198
openSNPrs443198
23andMers443198
23andMe allrs443198
SNP Nexus

SNPshotrs443198
SNPdbers443198
MSV3drs443198
GWAS Ctlgrs443198
GMAF0.4233
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21779181OA-icon.png]
Trait
Title Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
Risk Allele
P-val 9E-21
Odds Ratio 1.8200 [1.59-2.04]


[PMID 27231971] NOTCH4 gene polymorphisms as potential risk factors for brain arteriovenous malformation development and hemorrhagic presentation.