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rs1057517767

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs1057517767(-;-)
Make rs1057517767(-;GC)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47350534
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs1057517767
dbSNP (old)rs1057517767
ClinGenrs1057517767
ebirs1057517767
HLIrs1057517767
Exacrs1057517767
Gnomadrs1057517767
Varsomers1057517767
LitVarrs1057517767
Maprs1057517767
PheGenIrs1057517767
Biobankrs1057517767
1000 genomesrs1057517767
hgdprs1057517767
ensemblrs1057517767
gopubmedrs1057517767
geneviewrs1057517767
scholarrs1057517767
googlers1057517767
pharmgkbrs1057517767
gwascentralrs1057517767
openSNPrs1057517767
23andMers1057517767
23andMe allrs1057517767
SNPshotrs1057517767
SNPdbers1057517767
MSV3drs1057517767
GWAS Ctlgrs1057517767
Max Magnitude0
ClinVar
Risk rs1057517767(-;-)
Alt rs1057517767(-;-)
Reference Rs1057517767(GC;GC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372085_47372086delGC
CLNSRC
CLNACC RCV000414044.1,