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rs769392594

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs769392594(G;G)
Make rs769392594(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178608256
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs769392594
ebirs769392594
HLIrs769392594
Exacrs769392594
Varsomers769392594
Maprs769392594
PheGenIrs769392594
hapmaprs769392594
1000 genomesrs769392594
hgdprs769392594
ensemblrs769392594
gopubmedrs769392594
geneviewrs769392594
scholarrs769392594
googlers769392594
pharmgkbrs769392594
gwascentralrs769392594
openSNPrs769392594
23andMers769392594
23andMe allrs769392594
SNP Nexus

SNPshotrs769392594
SNPdbers769392594
MSV3drs769392594
GWAS Ctlgrs769392594
Max Magnitude0
ClinVar
Risk rs769392594(A,G;A,G)
Alt rs769392594(A,G;A,G)
Reference rs769392594(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179472983T>A
CLNSRC
CLNACC RCV000184234.1,