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rs370338674

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370338674(A;A)
Make rs370338674(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332099
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs370338674
ebirs370338674
HLIrs370338674
Exacrs370338674
Varsomers370338674
Maprs370338674
PheGenIrs370338674
hapmaprs370338674
1000 genomesrs370338674
hgdprs370338674
ensemblrs370338674
gopubmedrs370338674
geneviewrs370338674
scholarrs370338674
googlers370338674
pharmgkbrs370338674
gwascentralrs370338674
openSNPrs370338674
23andMers370338674
23andMe allrs370338674
SNP Nexus

SNPshotrs370338674
SNPdbers370338674
MSV3drs370338674
GWAS Ctlgrs370338674
Max Magnitude0
ClinVar
Risk rs370338674(A;A)
Alt rs370338674(A;A)
Reference rs370338674(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 0
HGVS NC_000011.9:g.47353650G>A
CLNSRC
CLNACC RCV000158265.2, RCV000177680.1,