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rs794727408

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727408(G;T)
Make rs794727408(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position216084697
GeneLOC102723833, USH2A
is asnp
is mentioned by
dbSNPrs794727408
ebirs794727408
HLIrs794727408
Exacrs794727408
Varsomers794727408
Maprs794727408
PheGenIrs794727408
hapmaprs794727408
1000 genomesrs794727408
hgdprs794727408
ensemblrs794727408
gopubmedrs794727408
geneviewrs794727408
scholarrs794727408
googlers794727408
pharmgkbrs794727408
gwascentralrs794727408
openSNPrs794727408
23andMers794727408
23andMe allrs794727408
SNP Nexus

SNPshotrs794727408
SNPdbers794727408
MSV3drs794727408
GWAS Ctlgrs794727408
Max Magnitude0
ClinVar
Risk rs794727408(T;T)
Alt rs794727408(T;T)
Reference rs794727408(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene LOC102723833 USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216258039C>A
CLNSRC
CLNACC RCV000176600.1,