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rs761807131

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761807131(C;T)
Make rs761807131(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178610089
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs761807131
ebirs761807131
HLIrs761807131
Exacrs761807131
Varsomers761807131
Maprs761807131
PheGenIrs761807131
hapmaprs761807131
1000 genomesrs761807131
hgdprs761807131
ensemblrs761807131
gopubmedrs761807131
geneviewrs761807131
scholarrs761807131
googlers761807131
pharmgkbrs761807131
gwascentralrs761807131
openSNPrs761807131
23andMers761807131
23andMe allrs761807131
SNP Nexus

SNPshotrs761807131
SNPdbers761807131
MSV3drs761807131
GWAS Ctlgrs761807131
Max Magnitude0
ClinVar
Risk rs761807131(T;T)
Alt rs761807131(T;T)
Reference rs761807131(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179474816C>T
CLNSRC
CLNACC RCV000184231.2,