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rs878855006

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855006(-;-)
Make rs878855006(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position53664993
GeneRPGRIP1L
is asnp
is mentioned by
dbSNPrs878855006
ebirs878855006
HLIrs878855006
Exacrs878855006
Varsomers878855006
Maprs878855006
PheGenIrs878855006
hapmaprs878855006
1000 genomesrs878855006
hgdprs878855006
ensemblrs878855006
gopubmedrs878855006
geneviewrs878855006
scholarrs878855006
googlers878855006
pharmgkbrs878855006
gwascentralrs878855006
openSNPrs878855006
23andMers878855006
23andMe allrs878855006
SNP Nexus

SNPshotrs878855006
SNPdbers878855006
MSV3drs878855006
GWAS Ctlgrs878855006
Max Magnitude0
ClinVar
Risk rs878855006(;)
Alt rs878855006(;)
Reference rs878855006(C;C)
Significance Pathogenic
Disease Familial aplasia of the vermis
Variation info
Gene RPGRIP1L
CLNDBN Familial aplasia of the vermis
Reversed 1
HGVS NC_000016.9:g.53698905delG
CLNSRC
CLNACC RCV000229421.1,