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rs794728467

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728467(-;GCGG)
Make rs794728467(GCGG;GCGG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947380
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728467
ClinGenrs794728467
ebirs794728467
HLIrs794728467
Exacrs794728467
Varsomers794728467
Maprs794728467
PheGenIrs794728467
hapmaprs794728467
1000 genomesrs794728467
hgdprs794728467
ensemblrs794728467
gopubmedrs794728467
geneviewrs794728467
scholarrs794728467
googlers794728467
pharmgkbrs794728467
gwascentralrs794728467
openSNPrs794728467
23andMers794728467
23andMe allrs794728467
SNP Nexus

SNPshotrs794728467
SNPdbers794728467
MSV3drs794728467
GWAS Ctlgrs794728467
Max Magnitude0
ClinVar
Risk rs794728467(GGCGGC;GGCGGC) Rs794728467(GCGGC;GCGGC)
Alt rs794728467(GGCGGC;GGCGGC) Rs794728467(GCGGC;GCGGC)
Reference Rs794728467(C;C)
Significance Pathogenic
Disease Cardiac arrhythmia not provided
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia not provided
Reversed 1
HGVS NC_000007.13:g.150644469_150644472dupCCGC; NC_000007.13:g.150644469_150644473dupCCGCC
CLNSRC
CLNACC RCV000182007.1, RCV000223868.1,