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rs797044511

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044511(A;G)
Make rs797044511(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77160980
GeneMYO7A
is asnp
is mentioned by
dbSNPrs797044511
ebirs797044511
HLIrs797044511
Exacrs797044511
Varsomers797044511
Maprs797044511
PheGenIrs797044511
hapmaprs797044511
1000 genomesrs797044511
hgdprs797044511
ensemblrs797044511
gopubmedrs797044511
geneviewrs797044511
scholarrs797044511
googlers797044511
pharmgkbrs797044511
gwascentralrs797044511
openSNPrs797044511
23andMers797044511
23andMe allrs797044511
SNP Nexus

SNPshotrs797044511
SNPdbers797044511
MSV3drs797044511
GWAS Ctlgrs797044511
Max Magnitude0
ClinVar
Risk rs797044511(G;G)
Alt rs797044511(G;G)
Reference rs797044511(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76872026A>G
CLNSRC
CLNACC RCV000155424.1,