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rs876657655

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657655(A;G)
Make rs876657655(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77211162
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657655
ebirs876657655
HLIrs876657655
Exacrs876657655
Varsomers876657655
Maprs876657655
PheGenIrs876657655
hapmaprs876657655
1000 genomesrs876657655
hgdprs876657655
ensemblrs876657655
gopubmedrs876657655
geneviewrs876657655
scholarrs876657655
googlers876657655
pharmgkbrs876657655
gwascentralrs876657655
openSNPrs876657655
23andMers876657655
23andMe allrs876657655
SNP Nexus

SNPshotrs876657655
SNPdbers876657655
MSV3drs876657655
GWAS Ctlgrs876657655
Max Magnitude0
ClinVar
Risk rs876657655(G;G)
Alt rs876657655(G;G)
Reference rs876657655(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76922207A>G
CLNSRC
CLNACC RCV000223094.1,