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rs143167166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143167166(A;A)
Make rs143167166(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150945375
GeneKCNH2
is asnp
is mentioned by
dbSNPrs143167166
ebirs143167166
HLIrs143167166
Exacrs143167166
Varsomers143167166
Maprs143167166
PheGenIrs143167166
hapmaprs143167166
1000 genomesrs143167166
hgdprs143167166
ensemblrs143167166
gopubmedrs143167166
geneviewrs143167166
scholarrs143167166
googlers143167166
pharmgkbrs143167166
gwascentralrs143167166
openSNPrs143167166
23andMers143167166
23andMe allrs143167166
SNP Nexus

SNPshotrs143167166
SNPdbers143167166
MSV3drs143167166
GWAS Ctlgrs143167166
Max Magnitude0
ClinVar
Risk rs143167166(A;A)
Alt rs143167166(A;A)
Reference rs143167166(G;G)
Significance Probable-Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME not specified
Variation info
Gene KCNH2
CLNDBN SUDDEN INFANT DEATH SYNDROME not specified
Reversed 0
HGVS NC_000007.13:g.150642463G>A
CLNSRC ClinVar
CLNACC RCV000058228.2, RCV000181918.2,