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rs794728449

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728449(-;GGGGC)
Make rs794728449(GGGGC;GGGGC)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947842
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728449
ClinGenrs794728449
ebirs794728449
HLIrs794728449
Exacrs794728449
Varsomers794728449
Maprs794728449
PheGenIrs794728449
hapmaprs794728449
1000 genomesrs794728449
hgdprs794728449
ensemblrs794728449
gopubmedrs794728449
geneviewrs794728449
scholarrs794728449
googlers794728449
pharmgkbrs794728449
gwascentralrs794728449
openSNPrs794728449
23andMers794728449
23andMe allrs794728449
SNP Nexus

SNPshotrs794728449
SNPdbers794728449
MSV3drs794728449
GWAS Ctlgrs794728449
Max Magnitude0
ClinVar
Risk rs794728449(GGGGC;GGGGC)
Alt rs794728449(GGGGC;GGGGC)
Reference Rs794728449(-;-)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644931_150644935dupGCCCC
CLNSRC
CLNACC RCV000181987.1,