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rs608781

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs608781(A;G)
Make rs608781(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position50880956
GeneME2
is asnp
is mentioned by
dbSNPrs608781
ebirs608781
HLIrs608781
Exacrs608781
Varsomers608781
Maprs608781
PheGenIrs608781
hapmaprs608781
1000 genomesrs608781
hgdprs608781
ensemblrs608781
gopubmedrs608781
geneviewrs608781
scholarrs608781
googlers608781
pharmgkbrs608781
gwascentralrs608781
openSNPrs608781
23andMers608781
23andMe allrs608781
SNP Nexus

SNPshotrs608781
SNPdbers608781
MSV3drs608781
GWAS Ctlgrs608781
GMAF0.1556
Max Magnitude0
OMIM154270
DescMALIC ENZYME 2; ME2
Variant
Relatedalso
OMIM154270
Desc
Variant0001
Relatedalso
[PMID 15532013OA-icon.png] Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy.