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rs786205540

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205540(G;T)
Make rs786205540(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178579663
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs786205540
ebirs786205540
HLIrs786205540
Exacrs786205540
Varsomers786205540
Maprs786205540
PheGenIrs786205540
hapmaprs786205540
1000 genomesrs786205540
hgdprs786205540
ensemblrs786205540
gopubmedrs786205540
geneviewrs786205540
scholarrs786205540
googlers786205540
pharmgkbrs786205540
gwascentralrs786205540
openSNPrs786205540
23andMers786205540
23andMe allrs786205540
SNP Nexus

SNPshotrs786205540
SNPdbers786205540
MSV3drs786205540
GWAS Ctlgrs786205540
Max Magnitude0
ClinVar
Risk rs786205540(T;T)
Alt rs786205540(T;T)
Reference rs786205540(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179444390C>A
CLNSRC
CLNACC RCV000171316.1,