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rs727503197

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs727503197(-;-)
Make rs727503197(-;GA)
Make rs727503197(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342081
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727503197
ebirs727503197
HLIrs727503197
Exacrs727503197
Varsomers727503197
Maprs727503197
PheGenIrs727503197
hapmaprs727503197
1000 genomesrs727503197
hgdprs727503197
ensemblrs727503197
gopubmedrs727503197
geneviewrs727503197
scholarrs727503197
googlers727503197
pharmgkbrs727503197
gwascentralrs727503197
openSNPrs727503197
23andMers727503197
23andMe allrs727503197
SNP Nexus

SNPshotrs727503197
SNPdbers727503197
MSV3drs727503197
GWAS Ctlgrs727503197
Max Magnitude0
ClinVar
Risk rs727503197(;)
Alt rs727503197(;)
Reference rs727503197(AG;AG)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47363631_47363632delCT
CLNSRC
CLNACC RCV000151117.2, RCV000158350.2,