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rs754921704

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754921704(G;T)
Make rs754921704(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974862
GeneKCNH2
is asnp
is mentioned by
dbSNPrs754921704
ebirs754921704
HLIrs754921704
Exacrs754921704
Varsomers754921704
Maprs754921704
PheGenIrs754921704
hapmaprs754921704
1000 genomesrs754921704
hgdprs754921704
ensemblrs754921704
gopubmedrs754921704
geneviewrs754921704
scholarrs754921704
googlers754921704
pharmgkbrs754921704
gwascentralrs754921704
openSNPrs754921704
23andMers754921704
23andMe allrs754921704
SNP Nexus

SNPshotrs754921704
SNPdbers754921704
MSV3drs754921704
GWAS Ctlgrs754921704
Max Magnitude0
ClinVar
Risk rs754921704(A,C,T;A,C,T)
Alt rs754921704(A,C,T;A,C,T)
Reference rs754921704(G;G)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 0
HGVS NC_000007.13:g.150671950G>T
CLNSRC
CLNACC RCV000182048.1,