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rs781811444

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781811444(C;T)
Make rs781811444(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77155908
GeneMYO7A
is asnp
is mentioned by
dbSNPrs781811444
ebirs781811444
HLIrs781811444
Exacrs781811444
Varsomers781811444
Maprs781811444
PheGenIrs781811444
hapmaprs781811444
1000 genomesrs781811444
hgdprs781811444
ensemblrs781811444
gopubmedrs781811444
geneviewrs781811444
scholarrs781811444
googlers781811444
pharmgkbrs781811444
gwascentralrs781811444
openSNPrs781811444
23andMers781811444
23andMe allrs781811444
SNP Nexus

SNPshotrs781811444
SNPdbers781811444
MSV3drs781811444
GWAS Ctlgrs781811444
Max Magnitude0
ClinVar
Risk rs781811444(T;T)
Alt rs781811444(T;T)
Reference rs781811444(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76866954C>T
CLNSRC
CLNACC RCV000156777.1,