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rs878853026

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853026(C;C)
Make rs878853026(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position210919966
GeneKCNH1
is asnp
is mentioned by
dbSNPrs878853026
ebirs878853026
HLIrs878853026
Exacrs878853026
Varsomers878853026
Maprs878853026
PheGenIrs878853026
hapmaprs878853026
1000 genomesrs878853026
hgdprs878853026
ensemblrs878853026
gopubmedrs878853026
geneviewrs878853026
scholarrs878853026
googlers878853026
pharmgkbrs878853026
gwascentralrs878853026
openSNPrs878853026
23andMers878853026
23andMe allrs878853026
SNP Nexus

SNPshotrs878853026
SNPdbers878853026
MSV3drs878853026
GWAS Ctlgrs878853026
Max Magnitude0
ClinVar
Risk rs878853026(C;C)
Alt rs878853026(C;C)
Reference rs878853026(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.211093308A>G
CLNSRC
CLNACC RCV000224297.1,