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rs199473541

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473541(A;G)
Make rs199473541(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947617
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473541
ebirs199473541
HLIrs199473541
Exacrs199473541
Varsomers199473541
Maprs199473541
PheGenIrs199473541
hapmaprs199473541
1000 genomesrs199473541
hgdprs199473541
ensemblrs199473541
gopubmedrs199473541
geneviewrs199473541
scholarrs199473541
googlers199473541
pharmgkbrs199473541
gwascentralrs199473541
openSNPrs199473541
23andMers199473541
23andMe allrs199473541
SNP Nexus

SNPshotrs199473541
SNPdbers199473541
MSV3drs199473541
GWAS Ctlgrs199473541
Max Magnitude0
ClinVar
Risk rs199473541(G;G)
Alt rs199473541(G;G)
Reference rs199473541(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644705T>C
CLNSRC ClinVar
CLNACC RCV000058183.2,