Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205541

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205541(A;A)
Make rs786205541(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178589395
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs786205541
ebirs786205541
HLIrs786205541
Exacrs786205541
Varsomers786205541
Maprs786205541
PheGenIrs786205541
hapmaprs786205541
1000 genomesrs786205541
hgdprs786205541
ensemblrs786205541
gopubmedrs786205541
geneviewrs786205541
scholarrs786205541
googlers786205541
pharmgkbrs786205541
gwascentralrs786205541
openSNPrs786205541
23andMers786205541
23andMe allrs786205541
SNP Nexus

SNPshotrs786205541
SNPdbers786205541
MSV3drs786205541
GWAS Ctlgrs786205541
Max Magnitude0
ClinVar
Risk rs786205541(A;A)
Alt rs786205541(A;A)
Reference rs786205541(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179454122C>T
CLNSRC
CLNACC RCV000171318.1,