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rs797044491

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044491(A;A)
Make rs797044491(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77158404
GeneMYO7A
is asnp
is mentioned by
dbSNPrs797044491
ebirs797044491
HLIrs797044491
Exacrs797044491
Varsomers797044491
Maprs797044491
PheGenIrs797044491
hapmaprs797044491
1000 genomesrs797044491
hgdprs797044491
ensemblrs797044491
gopubmedrs797044491
geneviewrs797044491
scholarrs797044491
googlers797044491
pharmgkbrs797044491
gwascentralrs797044491
openSNPrs797044491
23andMers797044491
23andMe allrs797044491
SNP Nexus

SNPshotrs797044491
SNPdbers797044491
MSV3drs797044491
GWAS Ctlgrs797044491
Max Magnitude0
ClinVar
Risk rs797044491(A;A)
Alt rs797044491(A;A)
Reference rs797044491(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76869450T>A
CLNSRC
CLNACC RCV000151482.1,