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rs369125667

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369125667(C;T)
Make rs369125667(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77142767
GeneMYO7A
is asnp
is mentioned by
dbSNPrs369125667
ebirs369125667
HLIrs369125667
Exacrs369125667
Varsomers369125667
Maprs369125667
PheGenIrs369125667
hapmaprs369125667
1000 genomesrs369125667
hgdprs369125667
ensemblrs369125667
gopubmedrs369125667
geneviewrs369125667
scholarrs369125667
googlers369125667
pharmgkbrs369125667
gwascentralrs369125667
openSNPrs369125667
23andMers369125667
23andMe allrs369125667
SNP Nexus

SNPshotrs369125667
SNPdbers369125667
MSV3drs369125667
GWAS Ctlgrs369125667
Max Magnitude0
ClinVar
Risk rs369125667(T;T)
Alt rs369125667(T;T)
Reference rs369125667(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76853813C>A
CLNSRC
CLNACC RCV000154340.1,