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rs773844428

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773844428(C;T)
Make rs773844428(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77208720
GeneMYO7A
is asnp
is mentioned by
dbSNPrs773844428
ebirs773844428
HLIrs773844428
Exacrs773844428
Varsomers773844428
Maprs773844428
PheGenIrs773844428
hapmaprs773844428
1000 genomesrs773844428
hgdprs773844428
ensemblrs773844428
gopubmedrs773844428
geneviewrs773844428
scholarrs773844428
googlers773844428
pharmgkbrs773844428
gwascentralrs773844428
openSNPrs773844428
23andMers773844428
23andMe allrs773844428
SNP Nexus

SNPshotrs773844428
SNPdbers773844428
MSV3drs773844428
GWAS Ctlgrs773844428
Max Magnitude0
ClinVar
Risk rs773844428(T;T)
Alt rs773844428(T;T)
Reference rs773844428(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76919765C>T
CLNSRC
CLNACC RCV000178544.1,