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rs771170000

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs771170000(C;C)
Make rs771170000(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position19360357
GeneB9D1
is asnp
is mentioned by
dbSNPrs771170000
ebirs771170000
HLIrs771170000
Exacrs771170000
Varsomers771170000
Maprs771170000
PheGenIrs771170000
hapmaprs771170000
1000 genomesrs771170000
hgdprs771170000
ensemblrs771170000
gopubmedrs771170000
geneviewrs771170000
scholarrs771170000
googlers771170000
pharmgkbrs771170000
gwascentralrs771170000
openSNPrs771170000
23andMers771170000
23andMe allrs771170000
SNP Nexus

SNPshotrs771170000
SNPdbers771170000
MSV3drs771170000
GWAS Ctlgrs771170000
Max Magnitude0
ClinVar
Risk rs771170000(C;C)
Alt rs771170000(C;C)
Reference rs771170000(T;T)
Significance Pathogenic
Disease Joubert syndrome
Variation info
Gene B9D1
CLNDBN Joubert syndrome
Reversed 0
HGVS NC_000017.10:g.19263670T>C
CLNSRC
CLNACC RCV000201685.1,