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rs876657415

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657415(-;-)
Make rs876657415(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77147888
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657415
ebirs876657415
HLIrs876657415
Exacrs876657415
Varsomers876657415
Maprs876657415
PheGenIrs876657415
hapmaprs876657415
1000 genomesrs876657415
hgdprs876657415
ensemblrs876657415
gopubmedrs876657415
geneviewrs876657415
scholarrs876657415
googlers876657415
pharmgkbrs876657415
gwascentralrs876657415
openSNPrs876657415
23andMers876657415
23andMe allrs876657415
SNP Nexus

SNPshotrs876657415
SNPdbers876657415
MSV3drs876657415
GWAS Ctlgrs876657415
Max Magnitude0
ClinVar
Risk rs876657415(;)
Alt rs876657415(;)
Reference rs876657415(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76858934delG
CLNSRC
CLNACC RCV000222769.1,