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rs770038577

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770038577(G;T)
Make rs770038577(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178561042
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs770038577
ebirs770038577
HLIrs770038577
Exacrs770038577
Varsomers770038577
Maprs770038577
PheGenIrs770038577
hapmaprs770038577
1000 genomesrs770038577
hgdprs770038577
ensemblrs770038577
gopubmedrs770038577
geneviewrs770038577
scholarrs770038577
googlers770038577
pharmgkbrs770038577
gwascentralrs770038577
openSNPrs770038577
23andMers770038577
23andMe allrs770038577
SNP Nexus

SNPshotrs770038577
SNPdbers770038577
MSV3drs770038577
GWAS Ctlgrs770038577
Max Magnitude0
ClinVar
Risk rs770038577(T;T)
Alt rs770038577(T;T)
Reference rs770038577(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179425769G>A
CLNSRC
CLNACC RCV000209383.1,