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rs876657654

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657654(G;G)
Make rs876657654(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77155935
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657654
ebirs876657654
HLIrs876657654
Exacrs876657654
Varsomers876657654
Maprs876657654
PheGenIrs876657654
hapmaprs876657654
1000 genomesrs876657654
hgdprs876657654
ensemblrs876657654
gopubmedrs876657654
geneviewrs876657654
scholarrs876657654
googlers876657654
pharmgkbrs876657654
gwascentralrs876657654
openSNPrs876657654
23andMers876657654
23andMe allrs876657654
SNP Nexus

SNPshotrs876657654
SNPdbers876657654
MSV3drs876657654
GWAS Ctlgrs876657654
Max Magnitude0
ClinVar
Risk rs876657654(G;G)
Alt rs876657654(G;G)
Reference rs876657654(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76866981T>G
CLNSRC
CLNACC RCV000219484.1,