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rs876657416

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657416(C;C)
Make rs876657416(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77174772
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657416
ebirs876657416
HLIrs876657416
Exacrs876657416
Varsomers876657416
Maprs876657416
PheGenIrs876657416
hapmaprs876657416
1000 genomesrs876657416
hgdprs876657416
ensemblrs876657416
gopubmedrs876657416
geneviewrs876657416
scholarrs876657416
googlers876657416
pharmgkbrs876657416
gwascentralrs876657416
openSNPrs876657416
23andMers876657416
23andMe allrs876657416
SNP Nexus

SNPshotrs876657416
SNPdbers876657416
MSV3drs876657416
GWAS Ctlgrs876657416
Max Magnitude0
ClinVar
Risk rs876657416(C;C)
Alt rs876657416(C;C)
Reference rs876657416(T;T)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76885818T>C
CLNSRC
CLNACC RCV000219432.1,