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rs1060499716

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499716(A;A)
Make rs1060499716(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position77157397
GeneMYO7A
is asnp
is mentioned by
dbSNPrs1060499716
dbSNP (old)rs1060499716
ClinGenrs1060499716
ebirs1060499716
HLIrs1060499716
Exacrs1060499716
Gnomadrs1060499716
Varsomers1060499716
Maprs1060499716
PheGenIrs1060499716
Biobankrs1060499716
1000 genomesrs1060499716
hgdprs1060499716
ensemblrs1060499716
gopubmedrs1060499716
geneviewrs1060499716
scholarrs1060499716
googlers1060499716
pharmgkbrs1060499716
gwascentralrs1060499716
openSNPrs1060499716
23andMers1060499716
23andMe allrs1060499716
SNPshotrs1060499716
SNPdbers1060499716
MSV3drs1060499716
GWAS Ctlgrs1060499716
Max Magnitude0
ClinVar
Risk rs1060499716(A;A)
Alt rs1060499716(A;A)
Reference Rs1060499716(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76868443G>A
CLNSRC
CLNACC RCV000449574.1,