rs1941958

Orientation

plus

Stabilized

plus

Make rs1941958(A;A)

Make rs1941958(A;G)

Make rs1941958(G;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

51200506

is a	snp
is	mentioned by
dbSNP	rs1941958
dbSNP (classic)	rs1941958
ClinGen	rs1941958
ebi	rs1941958
HLI	rs1941958
Exac	rs1941958
Gnomad	rs1941958
Varsome	rs1941958
LitVar	rs1941958
Map	rs1941958
PheGenI	rs1941958
Biobank	rs1941958
1000 genomes	rs1941958
hgdp	rs1941958
ensembl	rs1941958
geneview	rs1941958
scholar	rs1941958
google	rs1941958
pharmgkb	rs1941958
gwascentral	rs1941958
openSNP	rs1941958
23andMe	rs1941958
SNPshot	rs1941958
SNPdbe	rs1941958
MSV3d	rs1941958
GWAS Ctlg	rs1941958

GMAF

0.4972

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

OMIM	611014
Desc	HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8; HYT8
Variant
Related	also

OMIM	145500
Desc	HYPERTENSION, ESSENTIAL
Variant
Related	also

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