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rs386352318

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs386352318(G;G)
Make rs386352318(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position128911776
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs386352318
ebirs386352318
HLIrs386352318
Exacrs386352318
Varsomers386352318
Maprs386352318
PheGenIrs386352318
hapmaprs386352318
1000 genomesrs386352318
hgdprs386352318
ensemblrs386352318
gopubmedrs386352318
geneviewrs386352318
scholarrs386352318
googlers386352318
pharmgkbrs386352318
gwascentralrs386352318
openSNPrs386352318
23andMers386352318
23andMe allrs386352318
SNP Nexus

SNPshotrs386352318
SNPdbers386352318
MSV3drs386352318
GWAS Ctlgrs386352318
Max Magnitude0
ClinVar
Risk rs386352318(G;G)
Alt rs386352318(G;G)
Reference rs386352318(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNJ5
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.128781671T>G
CLNSRC
CLNACC RCV000122474.1,