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rs786205544

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205544(A;G)
Make rs786205544(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178721981
GeneTTN
is asnp
is mentioned by
dbSNPrs786205544
ebirs786205544
HLIrs786205544
Exacrs786205544
Varsomers786205544
Maprs786205544
PheGenIrs786205544
hapmaprs786205544
1000 genomesrs786205544
hgdprs786205544
ensemblrs786205544
gopubmedrs786205544
geneviewrs786205544
scholarrs786205544
googlers786205544
pharmgkbrs786205544
gwascentralrs786205544
openSNPrs786205544
23andMers786205544
23andMe allrs786205544
SNP Nexus

SNPshotrs786205544
SNPdbers786205544
MSV3drs786205544
GWAS Ctlgrs786205544
Max Magnitude0
ClinVar
Risk rs786205544(G;G)
Alt rs786205544(G;G)
Reference rs786205544(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179586708T>C
CLNSRC
CLNACC RCV000171323.1,