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rs1893379

From SNPedia

Orientationminus
Stabilizedminus
Make rs1893379(C;C)
Make rs1893379(C;T)
Make rs1893379(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position51192166
GeneMEX3C
is asnp
is mentioned by
dbSNPrs1893379
ebirs1893379
HLIrs1893379
Exacrs1893379
Varsomers1893379
Maprs1893379
PheGenIrs1893379
hapmaprs1893379
1000 genomesrs1893379
hgdprs1893379
ensemblrs1893379
gopubmedrs1893379
geneviewrs1893379
scholarrs1893379
googlers1893379
pharmgkbrs1893379
gwascentralrs1893379
openSNPrs1893379
23andMers1893379
23andMe allrs1893379
SNP Nexus

SNPshotrs1893379
SNPdbers1893379
MSV3drs1893379
GWAS Ctlgrs1893379
GMAF0.309
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM611014
DescHYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8; HYT8
Variant
Relatedalso
OMIM145500
DescHYPERTENSION, ESSENTIAL
Variant
Relatedalso
[PMID 15532013OA-icon.png] Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy.

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