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rs771203308

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771203308(C;T)
Make rs771203308(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position67158480
GeneCSPP1
is asnp
is mentioned by
dbSNPrs771203308
ebirs771203308
HLIrs771203308
Exacrs771203308
Varsomers771203308
Maprs771203308
PheGenIrs771203308
hapmaprs771203308
1000 genomesrs771203308
hgdprs771203308
ensemblrs771203308
gopubmedrs771203308
geneviewrs771203308
scholarrs771203308
googlers771203308
pharmgkbrs771203308
gwascentralrs771203308
openSNPrs771203308
23andMers771203308
23andMe allrs771203308
SNP Nexus

SNPshotrs771203308
SNPdbers771203308
MSV3drs771203308
GWAS Ctlgrs771203308
Max Magnitude0
ClinVar
Risk rs771203308(T;T)
Alt rs771203308(T;T)
Reference rs771203308(C;C)
Significance Pathogenic
Disease Joubert syndrome 21
Variation info
Gene CSPP1
CLNDBN Joubert syndrome 21
Reversed 0
HGVS NC_000008.10:g.68070715C>T
CLNSRC
CLNACC RCV000201785.1,