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rs786205536

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205536(C;C)
Make rs786205536(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178548813
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs786205536
ebirs786205536
HLIrs786205536
Exacrs786205536
Varsomers786205536
Maprs786205536
PheGenIrs786205536
hapmaprs786205536
1000 genomesrs786205536
hgdprs786205536
ensemblrs786205536
gopubmedrs786205536
geneviewrs786205536
scholarrs786205536
googlers786205536
pharmgkbrs786205536
gwascentralrs786205536
openSNPrs786205536
23andMers786205536
23andMe allrs786205536
SNP Nexus

SNPshotrs786205536
SNPdbers786205536
MSV3drs786205536
GWAS Ctlgrs786205536
Max Magnitude0
ClinVar
Risk rs786205536(C;C)
Alt rs786205536(C;C)
Reference rs786205536(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179413540C>G
CLNSRC
CLNACC RCV000171310.1,