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rs876657711

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876657711(-;-)
Make rs876657711(-;CT)
Make rs876657711(CT;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77189431
GeneMYO7A
is asnp
is mentioned by
dbSNPrs876657711
ebirs876657711
HLIrs876657711
Exacrs876657711
Varsomers876657711
Maprs876657711
PheGenIrs876657711
hapmaprs876657711
1000 genomesrs876657711
hgdprs876657711
ensemblrs876657711
gopubmedrs876657711
geneviewrs876657711
scholarrs876657711
googlers876657711
pharmgkbrs876657711
gwascentralrs876657711
openSNPrs876657711
23andMers876657711
23andMe allrs876657711
SNP Nexus

SNPshotrs876657711
SNPdbers876657711
MSV3drs876657711
GWAS Ctlgrs876657711
Max Magnitude0
ClinVar
Risk rs876657711(;)
Alt rs876657711(;)
Reference rs876657711(TC;TC)
Significance Pathogenic
Disease not provided Usher syndrome
Variation info
Gene MYO7A
CLNDBN not provided Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76900476_76900477delCT
CLNSRC
CLNACC RCV000171464.1, RCV000222358.1,