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rs781988557

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781988557(A;A)
Make rs781988557(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77181548
GeneMYO7A
is asnp
is mentioned by
dbSNPrs781988557
ebirs781988557
HLIrs781988557
Exacrs781988557
Varsomers781988557
Maprs781988557
PheGenIrs781988557
hapmaprs781988557
1000 genomesrs781988557
hgdprs781988557
ensemblrs781988557
gopubmedrs781988557
geneviewrs781988557
scholarrs781988557
googlers781988557
pharmgkbrs781988557
gwascentralrs781988557
openSNPrs781988557
23andMers781988557
23andMe allrs781988557
SNP Nexus

SNPshotrs781988557
SNPdbers781988557
MSV3drs781988557
GWAS Ctlgrs781988557
Max Magnitude0
ClinVar
Risk rs781988557(A;A)
Alt rs781988557(A;A)
Reference rs781988557(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76892594G>A
CLNSRC
CLNACC RCV000154343.1,