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rs577938494

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs577938494(C;C)
Make rs577938494(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position215675211
GeneUSH2A
is asnp
is mentioned by
dbSNPrs577938494
ebirs577938494
HLIrs577938494
Exacrs577938494
Varsomers577938494
Maprs577938494
PheGenIrs577938494
hapmaprs577938494
1000 genomesrs577938494
hgdprs577938494
ensemblrs577938494
gopubmedrs577938494
geneviewrs577938494
scholarrs577938494
googlers577938494
pharmgkbrs577938494
gwascentralrs577938494
openSNPrs577938494
23andMers577938494
23andMe allrs577938494
SNP Nexus

SNPshotrs577938494
SNPdbers577938494
MSV3drs577938494
GWAS Ctlgrs577938494
Max Magnitude0
ClinVar
Risk rs577938494(C;C)
Alt rs577938494(C;C)
Reference rs577938494(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 0
HGVS NC_000001.10:g.215848553T>G
CLNSRC
CLNACC RCV000221320.1,