Have questions? Visit https://www.reddit.com/r/SNPedia

rs1109771

From SNPedia

Orientationplus
Make rs1109771(A;A)
Make rs1109771(A;G)
Make rs1109771(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position32219828
GeneNOTCH4
is asnp
is mentioned by
dbSNPrs1109771
ebirs1109771
HLIrs1109771
Exacrs1109771
Varsomers1109771
Maprs1109771
PheGenIrs1109771
hapmaprs1109771
1000 genomesrs1109771
hgdprs1109771
ensemblrs1109771
gopubmedrs1109771
geneviewrs1109771
scholarrs1109771
googlers1109771
pharmgkbrs1109771
gwascentralrs1109771
openSNPrs1109771
23andMers1109771
23andMe allrs1109771
SNP Nexus

SNPshotrs1109771
SNPdbers1109771
MSV3drs1109771
GWAS Ctlgrs1109771
Max Magnitude
? (A;A) (A;G) (G;G) 28

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