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rs794728466

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCCCCGGGGCG;GCCCCGGGGCG) 0 common in clinvar
Make rs794728466(-;-)
Make rs794728466(-;GCCCCGGGGCG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947371
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728466
ClinGenrs794728466
ebirs794728466
HLIrs794728466
Exacrs794728466
Varsomers794728466
Maprs794728466
PheGenIrs794728466
hapmaprs794728466
1000 genomesrs794728466
hgdprs794728466
ensemblrs794728466
gopubmedrs794728466
geneviewrs794728466
scholarrs794728466
googlers794728466
pharmgkbrs794728466
gwascentralrs794728466
openSNPrs794728466
23andMers794728466
23andMe allrs794728466
SNP Nexus

SNPshotrs794728466
SNPdbers794728466
MSV3drs794728466
GWAS Ctlgrs794728466
Max Magnitude0
ClinVar
Risk rs794728466(-;-)
Alt rs794728466(-;-)
Reference Rs794728466(GCCCCGGGGCG;GCCCCGGGGCG)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644459_150644469delCGCCCCGGGGC
CLNSRC
CLNACC RCV000182006.2,