Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518195

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518195(C;T)
Make rs1057518195(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178535790
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1057518195
dbSNP (classic)rs1057518195
ClinGenrs1057518195
ebirs1057518195
HLIrs1057518195
Exacrs1057518195
Gnomadrs1057518195
Varsomers1057518195
LitVarrs1057518195
Maprs1057518195
PheGenIrs1057518195
Biobankrs1057518195
1000 genomesrs1057518195
hgdprs1057518195
ensemblrs1057518195
geneviewrs1057518195
scholarrs1057518195
googlers1057518195
pharmgkbrs1057518195
gwascentralrs1057518195
openSNPrs1057518195
23andMers1057518195
23andMe allrs1057518195
SNPshotrs1057518195
SNPdbers1057518195
MSV3drs1057518195
GWAS Ctlgrs1057518195
Max Magnitude0
ClinVar
Risk rs1057518195(T;T)
Alt rs1057518195(T;T)
Reference Rs1057518195(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179400517G>A
CLNSRC
CLNACC RCV000412935.1,