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rs1057517857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517857(C;T)
Make rs1057517857(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77190113
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1057517857
dbSNP (old)rs1057517857
ClinGenrs1057517857
ebirs1057517857
HLIrs1057517857
Exacrs1057517857
Gnomadrs1057517857
Varsomers1057517857
Maprs1057517857
PheGenIrs1057517857
Biobankrs1057517857
1000 genomesrs1057517857
hgdprs1057517857
ensemblrs1057517857
gopubmedrs1057517857
geneviewrs1057517857
scholarrs1057517857
googlers1057517857
pharmgkbrs1057517857
gwascentralrs1057517857
openSNPrs1057517857
23andMers1057517857
23andMe allrs1057517857
SNPshotrs1057517857
SNPdbers1057517857
MSV3drs1057517857
GWAS Ctlgrs1057517857
Max Magnitude0
ClinVar
Risk rs1057517857(T;T)
Alt rs1057517857(T;T)
Reference Rs1057517857(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYO7A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.76901158C>T
CLNSRC
CLNACC RCV000413055.1,