Have questions? Visit https://www.reddit.com/r/SNPedia

rs794726654

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726654(-;-)
Make rs794726654(-;GCTGTTT)
Make rs794726654(GCTGTTT;GCTGTTT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position120838843
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs794726654
ebirs794726654
HLIrs794726654
Exacrs794726654
Varsomers794726654
Maprs794726654
PheGenIrs794726654
hapmaprs794726654
1000 genomesrs794726654
hgdprs794726654
ensemblrs794726654
gopubmedrs794726654
geneviewrs794726654
scholarrs794726654
googlers794726654
pharmgkbrs794726654
gwascentralrs794726654
openSNPrs794726654
23andMers794726654
23andMe allrs794726654
SNP Nexus

SNPshotrs794726654
SNPdbers794726654
MSV3drs794726654
GWAS Ctlgrs794726654
Max Magnitude0
ClinVar
Risk rs794726654(GCTGTTTC,TC;GCTGTTTC,TC)
Alt rs794726654(GCTGTTTC,TC;GCTGTTTC,TC)
Reference rs794726654(C;C)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120478898_120478904dupAAACAGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000000349.7,