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rs863224941

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224941(C;G)
Make rs863224941(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position215799038
GeneUSH2A
is asnp
is mentioned by
dbSNPrs863224941
ebirs863224941
HLIrs863224941
Exacrs863224941
Varsomers863224941
Maprs863224941
PheGenIrs863224941
hapmaprs863224941
1000 genomesrs863224941
hgdprs863224941
ensemblrs863224941
gopubmedrs863224941
geneviewrs863224941
scholarrs863224941
googlers863224941
pharmgkbrs863224941
gwascentralrs863224941
openSNPrs863224941
23andMers863224941
23andMe allrs863224941
SNP Nexus

SNPshotrs863224941
SNPdbers863224941
MSV3drs863224941
GWAS Ctlgrs863224941
Max Magnitude0
ClinVar
Risk rs863224941(G;G)
Alt rs863224941(G;G)
Reference rs863224941(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.215972380G>C
CLNSRC
CLNACC RCV000200078.1,