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rs367990952

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367990952(A;A)
Make rs367990952(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351261
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs367990952
ebirs367990952
HLIrs367990952
Exacrs367990952
Varsomers367990952
Maprs367990952
PheGenIrs367990952
hapmaprs367990952
1000 genomesrs367990952
hgdprs367990952
ensemblrs367990952
gopubmedrs367990952
geneviewrs367990952
scholarrs367990952
googlers367990952
pharmgkbrs367990952
gwascentralrs367990952
openSNPrs367990952
23andMers367990952
23andMe allrs367990952
SNP Nexus

SNPshotrs367990952
SNPdbers367990952
MSV3drs367990952
GWAS Ctlgrs367990952
Max Magnitude0
ClinVar
Risk rs367990952(A;A)
Alt rs367990952(A;A)
Reference rs367990952(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47372812G>C
CLNSRC
CLNACC RCV000171196.1,