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rs767521596

From SNPedia

Orientationplus
Make rs767521596(-;-)
Make rs767521596(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959591
GeneKCNH2
is asnp
is mentioned by
dbSNPrs767521596
ebirs767521596
HLIrs767521596
Exacrs767521596
Varsomers767521596
Maprs767521596
PheGenIrs767521596
hapmaprs767521596
1000 genomesrs767521596
hgdprs767521596
ensemblrs767521596
gopubmedrs767521596
geneviewrs767521596
scholarrs767521596
googlers767521596
pharmgkbrs767521596
gwascentralrs767521596
openSNPrs767521596
23andMers767521596
23andMe allrs767521596
SNP Nexus

SNPshotrs767521596
SNPdbers767521596
MSV3drs767521596
GWAS Ctlgrs767521596
Max Magnitude
ClinVar
Risk rs767521596(;)
Alt rs767521596(;)
Reference rs767521596(G;G)
Significance Pathogenic
Disease not provided Long QT syndrome 2
Variation info
Gene KCNH2
CLNDBN not provided Long QT syndrome 2
Reversed 0
HGVS NC_000007.13:g.150656679delG
CLNSRC
CLNACC RCV000181956.2, RCV000208221.1,