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rs876657712

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657712(-;-)
Make rs876657712(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77198608
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657712
ebirs876657712
HLIrs876657712
Exacrs876657712
Varsomers876657712
Maprs876657712
PheGenIrs876657712
hapmaprs876657712
1000 genomesrs876657712
hgdprs876657712
ensemblrs876657712
gopubmedrs876657712
geneviewrs876657712
scholarrs876657712
googlers876657712
pharmgkbrs876657712
gwascentralrs876657712
openSNPrs876657712
23andMers876657712
23andMe allrs876657712
SNP Nexus

SNPshotrs876657712
SNPdbers876657712
MSV3drs876657712
GWAS Ctlgrs876657712
Max Magnitude0
ClinVar
Risk rs876657712(;)
Alt rs876657712(;)
Reference rs876657712(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76909653delG
CLNSRC
CLNACC RCV000216749.1,