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rs786205452

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205452(G;T)
Make rs786205452(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position216175450
GeneUSH2A
is asnp
is mentioned by
dbSNPrs786205452
ebirs786205452
HLIrs786205452
Exacrs786205452
Varsomers786205452
Maprs786205452
PheGenIrs786205452
hapmaprs786205452
1000 genomesrs786205452
hgdprs786205452
ensemblrs786205452
gopubmedrs786205452
geneviewrs786205452
scholarrs786205452
googlers786205452
pharmgkbrs786205452
gwascentralrs786205452
openSNPrs786205452
23andMers786205452
23andMe allrs786205452
SNP Nexus

SNPshotrs786205452
SNPdbers786205452
MSV3drs786205452
GWAS Ctlgrs786205452
Max Magnitude0
ClinVar
Risk rs786205452(T;T)
Alt rs786205452(T;T)
Reference rs786205452(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.216348792C>A
CLNSRC
CLNACC RCV000171168.1,