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rs1057520744

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520744(G;G)
Make rs1057520744(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178554863
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1057520744
dbSNP (classic)rs1057520744
ClinGenrs1057520744
ebirs1057520744
HLIrs1057520744
Exacrs1057520744
Gnomadrs1057520744
Varsomers1057520744
LitVarrs1057520744
Maprs1057520744
PheGenIrs1057520744
Biobankrs1057520744
1000 genomesrs1057520744
hgdprs1057520744
ensemblrs1057520744
geneviewrs1057520744
scholarrs1057520744
googlers1057520744
pharmgkbrs1057520744
gwascentralrs1057520744
openSNPrs1057520744
23andMers1057520744
SNPshotrs1057520744
SNPdbers1057520744
MSV3drs1057520744
GWAS Ctlgrs1057520744
Max Magnitude0
ClinVar
Risk rs1057520744(G;G)
Alt rs1057520744(G;G)
Reference Rs1057520744(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179419590A>C
CLNSRC
CLNACC RCV000433360.1,