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rs483352832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483352832(A;A)
Make rs483352832(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201364327
GeneTNNT2
is asnp
is mentioned by
dbSNPrs483352832
ebirs483352832
HLIrs483352832
Exacrs483352832
Varsomers483352832
Maprs483352832
PheGenIrs483352832
hapmaprs483352832
1000 genomesrs483352832
hgdprs483352832
ensemblrs483352832
gopubmedrs483352832
geneviewrs483352832
scholarrs483352832
googlers483352832
pharmgkbrs483352832
gwascentralrs483352832
openSNPrs483352832
23andMers483352832
23andMe allrs483352832
SNP Nexus

SNPshotrs483352832
SNPdbers483352832
MSV3drs483352832
GWAS Ctlgrs483352832
Max Magnitude0
ClinVar
Risk rs483352832(A;A)
Alt rs483352832(A;A)
Reference rs483352832(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1DD Cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Dilated cardiomyopathy 1DD Cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.201333455G>A
CLNSRC ClinVar
CLNACC RCV000119344.2, RCV000159338.1,