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rs56391938

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56391938(C;C)
Make rs56391938(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178568916
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs56391938
ebirs56391938
HLIrs56391938
Exacrs56391938
Varsomers56391938
Maprs56391938
PheGenIrs56391938
hapmaprs56391938
1000 genomesrs56391938
hgdprs56391938
ensemblrs56391938
gopubmedrs56391938
geneviewrs56391938
scholarrs56391938
googlers56391938
pharmgkbrs56391938
gwascentralrs56391938
openSNPrs56391938
23andMers56391938
23andMe allrs56391938
SNP Nexus

SNPshotrs56391938
SNPdbers56391938
MSV3drs56391938
GWAS Ctlgrs56391938
Max Magnitude0
ClinVar
Risk rs56391938(C;C)
Alt rs56391938(C;C)
Reference rs56391938(G;G)
Significance Probable-non-pathogenic
Disease not provided not specified Dilated cardiomyopathy 1G Limb-girdle muscular dystrophy
Variation info
Gene TTN TTN-AS1
CLNDBN not provided not specified Dilated cardiomyopathy 1G Limb-girdle muscular dystrophy, type 2J
Reversed 0
HGVS NC_000002.11:g.179433643G>C
CLNSRC
CLNACC RCV000172634.3, RCV000213073.2, RCV000228086.1,