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rs778533826

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778533826(A;A)
Make rs778533826(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position53619112
GeneRPGRIP1L
is asnp
is mentioned by
dbSNPrs778533826
ebirs778533826
HLIrs778533826
Exacrs778533826
Varsomers778533826
Maprs778533826
PheGenIrs778533826
hapmaprs778533826
1000 genomesrs778533826
hgdprs778533826
ensemblrs778533826
gopubmedrs778533826
geneviewrs778533826
scholarrs778533826
googlers778533826
pharmgkbrs778533826
gwascentralrs778533826
openSNPrs778533826
23andMers778533826
23andMe allrs778533826
SNP Nexus

SNPshotrs778533826
SNPdbers778533826
MSV3drs778533826
GWAS Ctlgrs778533826
Max Magnitude0
ClinVar
Risk rs778533826(A;A)
Alt rs778533826(A;A)
Reference rs778533826(G;G)
Significance Pathogenic
Disease Joubert syndrome 7
Variation info
Gene RPGRIP1L
CLNDBN Joubert syndrome 7
Reversed 0
HGVS NC_000016.9:g.53653024G>A
CLNSRC
CLNACC RCV000201661.1,