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

rs557312035

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs557312035(C;C)
Make rs557312035(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178564811
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs557312035
ebirs557312035
HLIrs557312035
Exacrs557312035
Varsomers557312035
Maprs557312035
PheGenIrs557312035
hapmaprs557312035
1000 genomesrs557312035
hgdprs557312035
ensemblrs557312035
gopubmedrs557312035
geneviewrs557312035
scholarrs557312035
googlers557312035
pharmgkbrs557312035
gwascentralrs557312035
openSNPrs557312035
23andMers557312035
23andMe allrs557312035
SNP Nexus

SNPshotrs557312035
SNPdbers557312035
MSV3drs557312035
GWAS Ctlgrs557312035
Max Magnitude0
ClinVar
Risk rs557312035(A,C,T;A,C,T)
Alt rs557312035(A,C,T;A,C,T)
Reference rs557312035(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179429538G>C
CLNSRC
CLNACC RCV000209674.2,