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rs41318021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41318021(C;T)
Make rs41318021(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position29514470
GeneSLC7A1
is asnp
is mentioned by
dbSNPrs41318021
ebirs41318021
HLIrs41318021
Exacrs41318021
Varsomers41318021
Maprs41318021
PheGenIrs41318021
hapmaprs41318021
1000 genomesrs41318021
hgdprs41318021
ensemblrs41318021
gopubmedrs41318021
geneviewrs41318021
scholarrs41318021
googlers41318021
pharmgkbrs41318021
gwascentralrs41318021
openSNPrs41318021
23andMers41318021
23andMe allrs41318021
SNP Nexus

SNPshotrs41318021
SNPdbers41318021
MSV3drs41318021
GWAS Ctlgrs41318021
GMAF0.03857
Max Magnitude0
[PMID 19067360] endothelial dysfunction seen in hypertensive subjects. notable that the authors initiated their own dbsnp entry and cite the ss# in the abstract as well as relating to microRNA


[PMID 23841815OA-icon.png] Contribution of SLC7A1 genetic variant to hypertension, the TAMRISK study