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rs587777285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777285(C;T)
Make rs587777285(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position120838776
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs587777285
ebirs587777285
HLIrs587777285
Exacrs587777285
Varsomers587777285
Maprs587777285
PheGenIrs587777285
hapmaprs587777285
1000 genomesrs587777285
hgdprs587777285
ensemblrs587777285
gopubmedrs587777285
geneviewrs587777285
scholarrs587777285
googlers587777285
pharmgkbrs587777285
gwascentralrs587777285
openSNPrs587777285
23andMers587777285
23andMe allrs587777285
SNP Nexus

SNPshotrs587777285
SNPdbers587777285
MSV3drs587777285
GWAS Ctlgrs587777285
Max Magnitude0
ClinVar
Risk rs587777285(C,T;C,T)
Alt rs587777285(C,T;C,T)
Reference rs587777285(G;G)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120478830C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000114401.4,