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rs10967705

From SNPedia

Orientationplus
Stabilizedplus
Make rs10967705(C;C)
Make rs10967705(C;G)
Make rs10967705(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome9
Position2717922
GeneKCNV2
is asnp
is mentioned by
dbSNPrs10967705
dbSNP (classic)rs10967705
ClinGenrs10967705
ebirs10967705
HLIrs10967705
Exacrs10967705
Gnomadrs10967705
Varsomers10967705
LitVarrs10967705
Maprs10967705
PheGenIrs10967705
Biobankrs10967705
1000 genomesrs10967705
hgdprs10967705
ensemblrs10967705
geneviewrs10967705
scholarrs10967705
googlers10967705
pharmgkbrs10967705
gwascentralrs10967705
openSNPrs10967705
23andMers10967705
SNPshotrs10967705
SNPdbers10967705
MSV3drs10967705
GWAS Ctlgrs10967705
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 30441785OA-icon.png] The Impact of Potassium Channel Gene Polymorphisms on Antiepileptic Drug Responsiveness in Arab Patients with Epilepsy.