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rs746837034

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746837034(C;T)
Make rs746837034(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position215648760
GeneUSH2A
is asnp
is mentioned by
dbSNPrs746837034
ebirs746837034
HLIrs746837034
Exacrs746837034
Varsomers746837034
Maprs746837034
PheGenIrs746837034
hapmaprs746837034
1000 genomesrs746837034
hgdprs746837034
ensemblrs746837034
gopubmedrs746837034
geneviewrs746837034
scholarrs746837034
googlers746837034
pharmgkbrs746837034
gwascentralrs746837034
openSNPrs746837034
23andMers746837034
23andMe allrs746837034
SNP Nexus

SNPshotrs746837034
SNPdbers746837034
MSV3drs746837034
GWAS Ctlgrs746837034
Max Magnitude0
ClinVar
Risk rs746837034(T;T)
Alt rs746837034(T;T)
Reference rs746837034(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene USH2A
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000001.10:g.215822102C>A
CLNSRC
CLNACC RCV000225551.1,