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rs730880642

From SNPedia

Orientationminus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs730880642(-;-)
Make rs730880642(-;GG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342876
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880642
ebirs730880642
HLIrs730880642
Exacrs730880642
Varsomers730880642
Maprs730880642
PheGenIrs730880642
hapmaprs730880642
1000 genomesrs730880642
hgdprs730880642
ensemblrs730880642
gopubmedrs730880642
geneviewrs730880642
scholarrs730880642
googlers730880642
pharmgkbrs730880642
gwascentralrs730880642
openSNPrs730880642
23andMers730880642
23andMe allrs730880642
SNP Nexus

SNPshotrs730880642
SNPdbers730880642
MSV3drs730880642
GWAS Ctlgrs730880642
Max Magnitude0
ClinVar
Risk rs730880642(;)
Alt rs730880642(;)
Reference rs730880642(GG;GG)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364427_47364428delCC
CLNSRC
CLNACC RCV000158345.1,