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rs727504247

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504247(A;A)
Make rs727504247(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201359217
GeneTNNT2
is asnp
is mentioned by
dbSNPrs727504247
ebirs727504247
HLIrs727504247
Exacrs727504247
Varsomers727504247
Maprs727504247
PheGenIrs727504247
hapmaprs727504247
1000 genomesrs727504247
hgdprs727504247
ensemblrs727504247
gopubmedrs727504247
geneviewrs727504247
scholarrs727504247
googlers727504247
pharmgkbrs727504247
gwascentralrs727504247
openSNPrs727504247
23andMers727504247
23andMe allrs727504247
SNP Nexus

SNPshotrs727504247
SNPdbers727504247
MSV3drs727504247
GWAS Ctlgrs727504247
Max Magnitude0
ClinVar
Risk rs727504247(A;A)
Alt rs727504247(A;A)
Reference rs727504247(G;G)
Significance Other
Disease Familial hypertrophic cardiomyopathy 2 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Familial hypertrophic cardiomyopathy 2 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201328345C>T
CLNSRC
CLNACC RCV000154218.5, RCV000159326.2, RCV000211869.1,