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rs1799762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0
Make rs1799762(-;G)
Make rs1799762(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position101126426
GeneSERPINE1
is asnp
is mentioned by
dbSNPrs1799762
ebirs1799762
HLIrs1799762
Exacrs1799762
Varsomers1799762
Maprs1799762
PheGenIrs1799762
hapmaprs1799762
1000 genomesrs1799762
hgdprs1799762
ensemblrs1799762
gopubmedrs1799762
geneviewrs1799762
scholarrs1799762
googlers1799762
pharmgkbrs1799762
gwascentralrs1799762
openSNPrs1799762
23andMers1799762
23andMe allrs1799762
SNP Nexus

SNPshotrs1799762
SNPdbers1799762
MSV3drs1799762
GWAS Ctlgrs1799762
Merged fromRs34857375, Rs72578597
GMAF0.4683
Max Magnitude0
This SNP is equivalent to, and therefore please go to, rs1799889 for related information.
Neighborrs34857375
Distance1
Neighborrs1799889
Distance2
[PMID 18603647OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.


[PMID 18805939OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.


[PMID 18936436OA-icon.png] Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.


[PMID 23274712OA-icon.png] Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.