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rs1057518008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518008(C;C)
Make rs1057518008(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position10638161
GeneMYH3
is asnp
is mentioned by
dbSNPrs1057518008
dbSNP (old)rs1057518008
ClinGenrs1057518008
ebirs1057518008
HLIrs1057518008
Exacrs1057518008
Gnomadrs1057518008
Varsomers1057518008
Maprs1057518008
PheGenIrs1057518008
Biobankrs1057518008
1000 genomesrs1057518008
hgdprs1057518008
ensemblrs1057518008
gopubmedrs1057518008
geneviewrs1057518008
scholarrs1057518008
googlers1057518008
pharmgkbrs1057518008
gwascentralrs1057518008
openSNPrs1057518008
23andMers1057518008
23andMe allrs1057518008
SNPshotrs1057518008
SNPdbers1057518008
MSV3drs1057518008
GWAS Ctlgrs1057518008
Max Magnitude0
ClinVar
Risk rs1057518008(C;C)
Alt rs1057518008(C;C)
Reference Rs1057518008(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH3
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.10541478A>G
CLNSRC
CLNACC RCV000413850.1,