Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518030

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518030(-;-)
Make rs1057518030(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47337769
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs1057518030
dbSNP (old)rs1057518030
ClinGenrs1057518030
ebirs1057518030
HLIrs1057518030
Exacrs1057518030
Gnomadrs1057518030
Varsomers1057518030
Maprs1057518030
PheGenIrs1057518030
Biobankrs1057518030
1000 genomesrs1057518030
hgdprs1057518030
ensemblrs1057518030
gopubmedrs1057518030
geneviewrs1057518030
scholarrs1057518030
googlers1057518030
pharmgkbrs1057518030
gwascentralrs1057518030
openSNPrs1057518030
23andMers1057518030
23andMe allrs1057518030
SNPshotrs1057518030
SNPdbers1057518030
MSV3drs1057518030
GWAS Ctlgrs1057518030
Max Magnitude0
ClinVar
Risk rs1057518030(-;-)
Alt rs1057518030(-;-)
Reference Rs1057518030(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359320delG
CLNSRC
CLNACC RCV000414101.1,