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rs1057517962

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517962(-;-)
Make rs1057517962(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77192200
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1057517962
dbSNP (old)rs1057517962
ClinGenrs1057517962
ebirs1057517962
HLIrs1057517962
Exacrs1057517962
Gnomadrs1057517962
Varsomers1057517962
Maprs1057517962
PheGenIrs1057517962
Biobankrs1057517962
1000 genomesrs1057517962
hgdprs1057517962
ensemblrs1057517962
gopubmedrs1057517962
geneviewrs1057517962
scholarrs1057517962
googlers1057517962
pharmgkbrs1057517962
gwascentralrs1057517962
openSNPrs1057517962
23andMers1057517962
23andMe allrs1057517962
SNPshotrs1057517962
SNPdbers1057517962
MSV3drs1057517962
GWAS Ctlgrs1057517962
Max Magnitude0
ClinVar
Risk rs1057517962(-;-)
Alt rs1057517962(-;-)
Reference Rs1057517962(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYO7A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.76903245delC
CLNSRC
CLNACC RCV000413681.1,