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rs1057518851

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518851(A;A)
Make rs1057518851(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178571565
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1057518851
dbSNP (classic)rs1057518851
ClinGenrs1057518851
ebirs1057518851
HLIrs1057518851
Exacrs1057518851
Gnomadrs1057518851
Varsomers1057518851
LitVarrs1057518851
Maprs1057518851
PheGenIrs1057518851
Biobankrs1057518851
1000 genomesrs1057518851
hgdprs1057518851
ensemblrs1057518851
geneviewrs1057518851
scholarrs1057518851
googlers1057518851
pharmgkbrs1057518851
gwascentralrs1057518851
openSNPrs1057518851
23andMers1057518851
SNPshotrs1057518851
SNPdbers1057518851
MSV3drs1057518851
GWAS Ctlgrs1057518851
Max Magnitude0
ClinVar
Risk rs1057518851(A;A)
Alt rs1057518851(A;A)
Reference Rs1057518851(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Myopathy
Reversed 1
HGVS NC_000002.11:g.179436292C>T
CLNSRC
CLNACC RCV000414758.1,