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rs878853358

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs878853358(-;-)
Make rs878853358(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position101243918
GeneIMPG2
is asnp
is mentioned by
dbSNPrs878853358
ebirs878853358
HLIrs878853358
Exacrs878853358
Varsomers878853358
Maprs878853358
PheGenIrs878853358
hapmaprs878853358
1000 genomesrs878853358
hgdprs878853358
ensemblrs878853358
gopubmedrs878853358
geneviewrs878853358
scholarrs878853358
googlers878853358
pharmgkbrs878853358
gwascentralrs878853358
openSNPrs878853358
23andMers878853358
23andMe allrs878853358
SNP Nexus

SNPshotrs878853358
SNPdbers878853358
MSV3drs878853358
GWAS Ctlgrs878853358
Max Magnitude0
ClinVar
Risk rs878853358(;)
Alt rs878853358(;)
Reference rs878853358(TG;TG)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene IMPG2
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000003.11:g.100962762_100962763delCA
CLNSRC
CLNACC RCV000225600.1,