Have questions? Visit https://www.reddit.com/r/SNPedia

rs121912992

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912992(C;G)
Make rs121912992(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position7565478
GeneDSP
is asnp
is mentioned by
dbSNPrs121912992
ebirs121912992
HLIrs121912992
Exacrs121912992
Varsomers121912992
Maprs121912992
PheGenIrs121912992
hapmaprs121912992
1000 genomesrs121912992
hgdprs121912992
ensemblrs121912992
gopubmedrs121912992
geneviewrs121912992
scholarrs121912992
googlers121912992
pharmgkbrs121912992
gwascentralrs121912992
openSNPrs121912992
23andMers121912992
23andMe allrs121912992
SNP Nexus

SNPshotrs121912992
SNPdbers121912992
MSV3drs121912992
GWAS Ctlgrs121912992
GMAF0.0004591
Max Magnitude0
OMIM125647
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912992(G,T;G,T)
Alt rs121912992(G,T;G,T)
Reference rs121912992(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not specified
Variation info
Gene DSP
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 8 not specified
Reversed 0
HGVS NC_000006.11:g.7565711C>G; NC_000006.11:g.7565711C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018332.28, RCV000168637.1,