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

rs368277535

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368277535(A;A)
Make rs368277535(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178527188
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs368277535
dbSNP (classic)rs368277535
ClinGenrs368277535
ebirs368277535
HLIrs368277535
Exacrs368277535
Gnomadrs368277535
Varsomers368277535
LitVarrs368277535
Maprs368277535
PheGenIrs368277535
Biobankrs368277535
1000 genomesrs368277535
hgdprs368277535
ensemblrs368277535
geneviewrs368277535
scholarrs368277535
googlers368277535
pharmgkbrs368277535
gwascentralrs368277535
openSNPrs368277535
23andMers368277535
SNPshotrs368277535
SNPdbers368277535
MSV3drs368277535
GWAS Ctlgrs368277535
Max Magnitude0
ClinVar
Risk rs368277535(A;A) rs368277535(T;T)
Alt rs368277535(A;A) rs368277535(T;T)
Reference Rs368277535(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000002.11:g.179391915C>A
CLNSRC
CLNACC RCV000303273.2, RCV000482600.1,