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rs727504277

From SNPedia

Orientationminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs727504277(-;-)
Make rs727504277(-;GGA)
Make rs727504277(GGA;GGA)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365285
GeneTNNT2
is asnp
is mentioned by
dbSNPrs727504277
ebirs727504277
HLIrs727504277
Exacrs727504277
Varsomers727504277
Maprs727504277
PheGenIrs727504277
hapmaprs727504277
1000 genomesrs727504277
hgdprs727504277
ensemblrs727504277
gopubmedrs727504277
geneviewrs727504277
scholarrs727504277
googlers727504277
pharmgkbrs727504277
gwascentralrs727504277
openSNPrs727504277
23andMers727504277
23andMe allrs727504277
SNP Nexus

SNPshotrs727504277
SNPdbers727504277
MSV3drs727504277
GWAS Ctlgrs727504277
Max Magnitude0
ClinVar
Risk rs727504277(;)
Alt rs727504277(;)
Reference rs727504277(GAG;GAG)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334413_201334415delTCC
CLNSRC
CLNACC RCV000154282.2,