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rs1941958

From SNPedia

Orientationplus
Stabilizedplus
Make rs1941958(A;A)
Make rs1941958(A;G)
Make rs1941958(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position51200506
is asnp
is mentioned by
dbSNPrs1941958
ebirs1941958
HLIrs1941958
Exacrs1941958
Varsomers1941958
Maprs1941958
PheGenIrs1941958
hapmaprs1941958
1000 genomesrs1941958
hgdprs1941958
ensemblrs1941958
gopubmedrs1941958
geneviewrs1941958
scholarrs1941958
googlers1941958
pharmgkbrs1941958
gwascentralrs1941958
openSNPrs1941958
23andMers1941958
23andMe allrs1941958
SNP Nexus

SNPshotrs1941958
SNPdbers1941958
MSV3drs1941958
GWAS Ctlgrs1941958
GMAF0.4972
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM611014
DescHYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8; HYT8
Variant
Relatedalso
OMIM145500
DescHYPERTENSION, ESSENTIAL
Variant
Relatedalso


[PMID 17015768] Implication of chromosome 18 in hypertension by sibling pair and association analyses: putative involvement of the RKHD2 gene.