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rs760107623

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760107623(C;T)
Make rs760107623(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178528396
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs760107623
ebirs760107623
HLIrs760107623
Exacrs760107623
Varsomers760107623
Maprs760107623
PheGenIrs760107623
hapmaprs760107623
1000 genomesrs760107623
hgdprs760107623
ensemblrs760107623
gopubmedrs760107623
geneviewrs760107623
scholarrs760107623
googlers760107623
pharmgkbrs760107623
gwascentralrs760107623
openSNPrs760107623
23andMers760107623
23andMe allrs760107623
SNP Nexus

SNPshotrs760107623
SNPdbers760107623
MSV3drs760107623
GWAS Ctlgrs760107623
Max Magnitude0
ClinVar
Risk rs760107623(T;T)
Alt rs760107623(T;T)
Reference rs760107623(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179393123C>T
CLNSRC
CLNACC RCV000171307.1,