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rs727503636

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503636(A;A)
Make rs727503636(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178689052
GeneTTN
is asnp
is mentioned by
dbSNPrs727503636
ebirs727503636
HLIrs727503636
Exacrs727503636
Varsomers727503636
Maprs727503636
PheGenIrs727503636
hapmaprs727503636
1000 genomesrs727503636
hgdprs727503636
ensemblrs727503636
gopubmedrs727503636
geneviewrs727503636
scholarrs727503636
googlers727503636
pharmgkbrs727503636
gwascentralrs727503636
openSNPrs727503636
23andMers727503636
23andMe allrs727503636
SNP Nexus

SNPshotrs727503636
SNPdbers727503636
MSV3drs727503636
GWAS Ctlgrs727503636
Max Magnitude0
ClinVar
Risk rs727503636(A;A)
Alt rs727503636(A;A)
Reference rs727503636(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 1
HGVS NC_000002.11:g.179553779C>T
CLNSRC
CLNACC RCV000152375.1, RCV000184202.2,