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rs1739843

From SNPedia

Orientationplus
Stabilizedplus
Make rs1739843(C;C)
Make rs1739843(C;T)
Make rs1739843(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position16016759
GeneHSPB7
is asnp
is mentioned by
dbSNPrs1739843
ebirs1739843
HLIrs1739843
Exacrs1739843
Varsomers1739843
Maprs1739843
PheGenIrs1739843
hapmaprs1739843
1000 genomesrs1739843
hgdprs1739843
ensemblrs1739843
gopubmedrs1739843
geneviewrs1739843
scholarrs1739843
googlers1739843
pharmgkbrs1739843
gwascentralrs1739843
openSNPrs1739843
23andMers1739843
23andMe allrs1739843
SNP Nexus

SNPshotrs1739843
SNPdbers1739843
MSV3drs1739843
GWAS Ctlgrs1739843
GMAF0.359
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20124441OA-icon.png] Common variants in HSPB7 and FRMD4B associated with advanced heart failure


[PMID 20975947OA-icon.png] Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy


[PMID 17510212] Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension.


[PMID 23570452OA-icon.png] Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population


[PMID 25785112OA-icon.png] Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population