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

rs1057517766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs1057517766(-;-)
Make rs1057517766(-;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47351255
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs1057517766
dbSNP (classic)rs1057517766
ClinGenrs1057517766
ebirs1057517766
HLIrs1057517766
Exacrs1057517766
Gnomadrs1057517766
Varsomers1057517766
LitVarrs1057517766
Maprs1057517766
PheGenIrs1057517766
Biobankrs1057517766
1000 genomesrs1057517766
hgdprs1057517766
ensemblrs1057517766
geneviewrs1057517766
scholarrs1057517766
googlers1057517766
pharmgkbrs1057517766
gwascentralrs1057517766
openSNPrs1057517766
23andMers1057517766
23andMe allrs1057517766
SNPshotrs1057517766
SNPdbers1057517766
MSV3drs1057517766
GWAS Ctlgrs1057517766
Max Magnitude0
ClinVar
Risk rs1057517766(-;-)
Alt rs1057517766(-;-)
Reference Rs1057517766(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372806_47372807delGA
CLNSRC
CLNACC RCV000413465.1,