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rs1057519160

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519160(A;A)
Make rs1057519160(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178711235
GeneTTN
is asnp
is mentioned by
dbSNPrs1057519160
dbSNP (old)rs1057519160
ClinGenrs1057519160
ebirs1057519160
HLIrs1057519160
Exacrs1057519160
Gnomadrs1057519160
Varsomers1057519160
Maprs1057519160
PheGenIrs1057519160
Biobankrs1057519160
1000 genomesrs1057519160
hgdprs1057519160
ensemblrs1057519160
gopubmedrs1057519160
geneviewrs1057519160
scholarrs1057519160
googlers1057519160
pharmgkbrs1057519160
gwascentralrs1057519160
openSNPrs1057519160
23andMers1057519160
23andMe allrs1057519160
SNPshotrs1057519160
SNPdbers1057519160
MSV3drs1057519160
GWAS Ctlgrs1057519160
Max Magnitude0
ClinVar
Risk rs1057519160(A;A)
Alt rs1057519160(A;A)
Reference Rs1057519160(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179575962C>T
CLNSRC
CLNACC RCV000416209.2,