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rs727504198

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504198(G;T)
Make rs727504198(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178636764
GeneTTN
is asnp
is mentioned by
dbSNPrs727504198
ebirs727504198
HLIrs727504198
Exacrs727504198
Varsomers727504198
Maprs727504198
PheGenIrs727504198
hapmaprs727504198
1000 genomesrs727504198
hgdprs727504198
ensemblrs727504198
gopubmedrs727504198
geneviewrs727504198
scholarrs727504198
googlers727504198
pharmgkbrs727504198
gwascentralrs727504198
openSNPrs727504198
23andMers727504198
23andMe allrs727504198
SNP Nexus

SNPshotrs727504198
SNPdbers727504198
MSV3drs727504198
GWAS Ctlgrs727504198
Max Magnitude0
ClinVar
Risk rs727504198(A,T;A,T)
Alt rs727504198(A,T;A,T)
Reference rs727504198(G;G)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 1G
Variation info
Gene TTN
CLNDBN not provided Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179501491C>A; NC_000002.11:g.179501491C>T
CLNSRC
CLNACC RCV000154075.2, RCV000175258.1, RCV000184501.1,