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rs878853357

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853357(G;T)
Make rs878853357(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position101228876
GeneIMPG2
is asnp
is mentioned by
dbSNPrs878853357
ebirs878853357
HLIrs878853357
Exacrs878853357
Varsomers878853357
Maprs878853357
PheGenIrs878853357
hapmaprs878853357
1000 genomesrs878853357
hgdprs878853357
ensemblrs878853357
gopubmedrs878853357
geneviewrs878853357
scholarrs878853357
googlers878853357
pharmgkbrs878853357
gwascentralrs878853357
openSNPrs878853357
23andMers878853357
23andMe allrs878853357
SNP Nexus

SNPshotrs878853357
SNPdbers878853357
MSV3drs878853357
GWAS Ctlgrs878853357
Max Magnitude0
ClinVar
Risk rs878853357(T;T)
Alt rs878853357(T;T)
Reference rs878853357(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene IMPG2
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000003.11:g.100947720C>A
CLNSRC
CLNACC RCV000225458.1,