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rs876657417

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657417(C;C)
Make rs876657417(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77213978
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657417
ebirs876657417
HLIrs876657417
Exacrs876657417
Varsomers876657417
Maprs876657417
PheGenIrs876657417
hapmaprs876657417
1000 genomesrs876657417
hgdprs876657417
ensemblrs876657417
gopubmedrs876657417
geneviewrs876657417
scholarrs876657417
googlers876657417
pharmgkbrs876657417
gwascentralrs876657417
openSNPrs876657417
23andMers876657417
23andMe allrs876657417
SNP Nexus

SNPshotrs876657417
SNPdbers876657417
MSV3drs876657417
GWAS Ctlgrs876657417
Max Magnitude0
ClinVar
Risk rs876657417(C;C)
Alt rs876657417(C;C)
Reference rs876657417(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76925023T>C
CLNSRC
CLNACC RCV000220295.1,