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rs727505337

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505337(G;T)
Make rs727505337(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position215743285
GeneUSH2A
is asnp
is mentioned by
dbSNPrs727505337
ebirs727505337
HLIrs727505337
Exacrs727505337
Varsomers727505337
Maprs727505337
PheGenIrs727505337
hapmaprs727505337
1000 genomesrs727505337
hgdprs727505337
ensemblrs727505337
gopubmedrs727505337
geneviewrs727505337
scholarrs727505337
googlers727505337
pharmgkbrs727505337
gwascentralrs727505337
openSNPrs727505337
23andMers727505337
23andMe allrs727505337
SNP Nexus

SNPshotrs727505337
SNPdbers727505337
MSV3drs727505337
GWAS Ctlgrs727505337
Max Magnitude0
ClinVar
Risk rs727505337(T;T)
Alt rs727505337(T;T)
Reference rs727505337(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.215916627C>A
CLNSRC
CLNACC RCV000156887.1,