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rs199473377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473377(C;C)
Make rs199473377(C;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175470
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473377
ebirs199473377
HLIrs199473377
Exacrs199473377
Varsomers199473377
Maprs199473377
PheGenIrs199473377
hapmaprs199473377
1000 genomesrs199473377
hgdprs199473377
ensemblrs199473377
gopubmedrs199473377
geneviewrs199473377
scholarrs199473377
googlers199473377
pharmgkbrs199473377
gwascentralrs199473377
openSNPrs199473377
23andMers199473377
23andMe allrs199473377
SNP Nexus

SNPshotrs199473377
SNPdbers199473377
MSV3drs199473377
GWAS Ctlgrs199473377
Max Magnitude0
ClinVar
Risk rs199473377(A,C;A,C)
Alt rs199473377(A,C;A,C)
Reference rs199473377(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171611G>A; NC_000017.10:g.68171611G>C
CLNSRC ClinVar
CLNACC RCV000058312.2, RCV000058313.2,