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rs776595927

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776595927(G;T)
Make rs776595927(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947619
GeneKCNH2
is asnp
is mentioned by
dbSNPrs776595927
ebirs776595927
HLIrs776595927
Exacrs776595927
Varsomers776595927
Maprs776595927
PheGenIrs776595927
hapmaprs776595927
1000 genomesrs776595927
hgdprs776595927
ensemblrs776595927
gopubmedrs776595927
geneviewrs776595927
scholarrs776595927
googlers776595927
pharmgkbrs776595927
gwascentralrs776595927
openSNPrs776595927
23andMers776595927
23andMe allrs776595927
SNP Nexus

SNPshotrs776595927
SNPdbers776595927
MSV3drs776595927
GWAS Ctlgrs776595927
Max Magnitude0
ClinVar
Risk rs776595927(A,T;A,T)
Alt rs776595927(A,T;A,T)
Reference rs776595927(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150644707G>T
CLNSRC
CLNACC RCV000181902.2,