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rs1064796130

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CACT;CACT) 0 common in clinvar
Chromosome11
Position77182110
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1064796130
dbSNP (old)rs1064796130
ClinGenrs1064796130
ebirs1064796130
HLIrs1064796130
Exacrs1064796130
Gnomadrs1064796130
Varsomers1064796130
Maprs1064796130
PheGenIrs1064796130
Biobankrs1064796130
1000 genomesrs1064796130
hgdprs1064796130
ensemblrs1064796130
gopubmedrs1064796130
geneviewrs1064796130
scholarrs1064796130
googlers1064796130
pharmgkbrs1064796130
gwascentralrs1064796130
openSNPrs1064796130
23andMers1064796130
23andMe allrs1064796130
SNPshotrs1064796130
SNPdbers1064796130
MSV3drs1064796130
GWAS Ctlgrs1064796130
Max Magnitude0
ClinVar
Risk rs1064796130(-;-)
Alt rs1064796130(-;-)
Reference Rs1064796130(CACT;CACT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYO7A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.76893156_76893159delCTCA
CLNSRC
CLNACC RCV000484218.1,