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rs369488112

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369488112(A;A)
Make rs369488112(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position19343796
GeneB9D1
is asnp
is mentioned by
dbSNPrs369488112
ebirs369488112
HLIrs369488112
Exacrs369488112
Varsomers369488112
Maprs369488112
PheGenIrs369488112
hapmaprs369488112
1000 genomesrs369488112
hgdprs369488112
ensemblrs369488112
gopubmedrs369488112
geneviewrs369488112
scholarrs369488112
googlers369488112
pharmgkbrs369488112
gwascentralrs369488112
openSNPrs369488112
23andMers369488112
23andMe allrs369488112
SNP Nexus

SNPshotrs369488112
SNPdbers369488112
MSV3drs369488112
GWAS Ctlgrs369488112
Max Magnitude0
ClinVar
Risk rs369488112(A;A)
Alt rs369488112(A;A)
Reference rs369488112(G;G)
Significance Pathogenic
Disease Joubert syndrome
Variation info
Gene B9D1
CLNDBN Joubert syndrome
Reversed 0
HGVS NC_000017.10:g.19247109G>A
CLNSRC
CLNACC RCV000201564.1,