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rs773954226

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773954226(G;T)
Make rs773954226(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position67179927
GeneARFGEF1, CSPP1
is asnp
is mentioned by
dbSNPrs773954226
ebirs773954226
HLIrs773954226
Exacrs773954226
Varsomers773954226
Maprs773954226
PheGenIrs773954226
hapmaprs773954226
1000 genomesrs773954226
hgdprs773954226
ensemblrs773954226
gopubmedrs773954226
geneviewrs773954226
scholarrs773954226
googlers773954226
pharmgkbrs773954226
gwascentralrs773954226
openSNPrs773954226
23andMers773954226
23andMe allrs773954226
SNP Nexus

SNPshotrs773954226
SNPdbers773954226
MSV3drs773954226
GWAS Ctlgrs773954226
Max Magnitude0
ClinVar
Risk rs773954226(T;T)
Alt rs773954226(T;T)
Reference rs773954226(G;G)
Significance Pathogenic
Disease Joubert syndrome 21
Variation info
Gene CSPP1 ARFGEF1
CLNDBN Joubert syndrome 21
Reversed 0
HGVS NC_000008.10:g.68092162G>A
CLNSRC
CLNACC RCV000201570.1,