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rs1057519237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519237(C;T)
Make rs1057519237(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178702634
GeneTTN
is asnp
is mentioned by
dbSNPrs1057519237
dbSNP (old)rs1057519237
ClinGenrs1057519237
ebirs1057519237
HLIrs1057519237
Exacrs1057519237
Gnomadrs1057519237
Varsomers1057519237
Maprs1057519237
PheGenIrs1057519237
Biobankrs1057519237
1000 genomesrs1057519237
hgdprs1057519237
ensemblrs1057519237
gopubmedrs1057519237
geneviewrs1057519237
scholarrs1057519237
googlers1057519237
pharmgkbrs1057519237
gwascentralrs1057519237
openSNPrs1057519237
23andMers1057519237
23andMe allrs1057519237
SNPshotrs1057519237
SNPdbers1057519237
MSV3drs1057519237
GWAS Ctlgrs1057519237
Max Magnitude0
ClinVar
Risk rs1057519237(T;T)
Alt rs1057519237(T;T)
Reference Rs1057519237(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179567361G>A
CLNSRC
CLNACC RCV000415992.1,