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rs766590491

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766590491(A;A)
Make rs766590491(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position215867112
GeneUSH2A
is asnp
is mentioned by
dbSNPrs766590491
ebirs766590491
HLIrs766590491
Exacrs766590491
Varsomers766590491
Maprs766590491
PheGenIrs766590491
hapmaprs766590491
1000 genomesrs766590491
hgdprs766590491
ensemblrs766590491
gopubmedrs766590491
geneviewrs766590491
scholarrs766590491
googlers766590491
pharmgkbrs766590491
gwascentralrs766590491
openSNPrs766590491
23andMers766590491
23andMe allrs766590491
SNP Nexus

SNPshotrs766590491
SNPdbers766590491
MSV3drs766590491
GWAS Ctlgrs766590491
Max Magnitude0
ClinVar
Risk rs766590491(A;A)
Alt rs766590491(A;A)
Reference rs766590491(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 0
HGVS NC_000001.10:g.216040454G>A
CLNSRC
CLNACC RCV000213731.1,