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

rs770767998

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770767998(G;T)
Make rs770767998(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178629441
GeneTTN
is asnp
is mentioned by
dbSNPrs770767998
ebirs770767998
HLIrs770767998
Exacrs770767998
Varsomers770767998
Maprs770767998
PheGenIrs770767998
hapmaprs770767998
1000 genomesrs770767998
hgdprs770767998
ensemblrs770767998
gopubmedrs770767998
geneviewrs770767998
scholarrs770767998
googlers770767998
pharmgkbrs770767998
gwascentralrs770767998
openSNPrs770767998
23andMers770767998
23andMe allrs770767998
SNP Nexus

SNPshotrs770767998
SNPdbers770767998
MSV3drs770767998
GWAS Ctlgrs770767998
Max Magnitude0
ClinVar
Risk rs770767998(T;T)
Alt rs770767998(T;T)
Reference rs770767998(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179494168G>A
CLNSRC
CLNACC RCV000209591.1,