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rs1017

From SNPedia

Orientationplus
Stabilizedplus
Make rs1017(A;A)
Make rs1017(A;T)
Make rs1017(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position51394261
GeneISL1
is asnp
is mentioned by
dbSNPrs1017
ebirs1017
HLIrs1017
Exacrs1017
Varsomers1017
Maprs1017
PheGenIrs1017
hapmaprs1017
1000 genomesrs1017
hgdprs1017
ensemblrs1017
gopubmedrs1017
geneviewrs1017
scholarrs1017
googlers1017
pharmgkbrs1017
gwascentralrs1017
openSNPrs1017
23andMers1017
23andMe allrs1017
SNP Nexus

SNPshotrs1017
SNPdbers1017
MSV3drs1017
GWAS Ctlgrs1017
GMAF0.3669
Max Magnitude

[PMID 22480195OA-icon.png] ISL1 Common Variant rs1017 Is Not Associated with Susceptibility to Congenital Heart Disease in a Chinese Population [PMID 20520780OA-icon.png] Common variation in ISL1 confers genetic susceptibility for human congenital heart disease. [PMID 23229290] Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.


[PMID 23572340] Association between ISL1 variants and susceptibility to ventricular septal defect in a Chinese cohort.