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rs878853379

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853379(A;A)
Make rs878853379(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position150972611
GeneCLRN1, CLRN1-AS1
is asnp
is mentioned by
dbSNPrs878853379
ebirs878853379
HLIrs878853379
Exacrs878853379
Varsomers878853379
Maprs878853379
PheGenIrs878853379
hapmaprs878853379
1000 genomesrs878853379
hgdprs878853379
ensemblrs878853379
gopubmedrs878853379
geneviewrs878853379
scholarrs878853379
googlers878853379
pharmgkbrs878853379
gwascentralrs878853379
openSNPrs878853379
23andMers878853379
23andMe allrs878853379
SNP Nexus

SNPshotrs878853379
SNPdbers878853379
MSV3drs878853379
GWAS Ctlgrs878853379
Max Magnitude0
ClinVar
Risk rs878853379(A;A)
Alt rs878853379(A;A)
Reference rs878853379(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene CLRN1-AS1 CLRN1
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000003.11:g.150690398C>T
CLNSRC
CLNACC RCV000225684.1,