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rs1043994

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A)  ?
(A;G)  ?
(G;G) 0 common
ReferenceGRCh38 38.1/141
Chromosome19
Position15192033
GeneNOTCH3
is asnp
is mentioned by
dbSNPrs1043994
ebirs1043994
HLIrs1043994
Exacrs1043994
Varsomers1043994
Maprs1043994
PheGenIrs1043994
hapmaprs1043994
1000 genomesrs1043994
hgdprs1043994
ensemblrs1043994
gopubmedrs1043994
geneviewrs1043994
scholarrs1043994
googlers1043994
pharmgkbrs1043994
gwascentralrs1043994
openSNPrs1043994
23andMers1043994
23andMe allrs1043994
SNP Nexus

SNPshotrs1043994
SNPdbers1043994
MSV3drs1043994
GWAS Ctlgrs1043994
GMAF0.1442
Max Magnitude0
A study of ~100 German patients suffering from migraines reported SNP rs1043994 to be significantly associated with increased risk. [PMID 16426270]
Neighborrs28933697
Distance62
[PMID 22006983OA-icon.png] Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.

[PMID 22373597] Two novel mutations and a previously unreported intronic polymorphism in the NOTCH3 gene.


[PMID 25120811OA-icon.png] Notch1 single nucleotide polymorphism rs3124591 is associated with the risk of development of invasive ductal breast carcinoma in a Chinese population