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rs794726655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ACCAG;ACCAG) 0 common in clinvar
Make rs794726655(-;-)
Make rs794726655(-;ACCAG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position120810571
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs794726655
dbSNP (old)rs794726655
ClinGenrs794726655
ebirs794726655
HLIrs794726655
Exacrs794726655
Gnomadrs794726655
Varsomers794726655
Maprs794726655
PheGenIrs794726655
Biobankrs794726655
1000 genomesrs794726655
hgdprs794726655
ensemblrs794726655
gopubmedrs794726655
geneviewrs794726655
scholarrs794726655
googlers794726655
pharmgkbrs794726655
gwascentralrs794726655
openSNPrs794726655
23andMers794726655
23andMe allrs794726655
SNP Nexus

SNPshotrs794726655
SNPdbers794726655
MSV3drs794726655
GWAS Ctlgrs794726655
Max Magnitude0
ClinVar
Risk rs794726655(-;-)
Alt rs794726655(-;-)
Reference Rs794726655(ACCAG;ACCAG)
Significance Pathogenic
Disease Exudative vitreoretinopathy 5
Variation info
Gene TSPAN12
CLNDBN Exudative vitreoretinopathy 5
Reversed 1
HGVS NC_000007.13:g.120450625_120450629delCTGGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000351.7,