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rs757863670

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757863670(A;G)
Make rs757863670(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position41358004
GeneB9D2
is asnp
is mentioned by
dbSNPrs757863670
ebirs757863670
HLIrs757863670
Exacrs757863670
Varsomers757863670
Maprs757863670
PheGenIrs757863670
hapmaprs757863670
1000 genomesrs757863670
hgdprs757863670
ensemblrs757863670
gopubmedrs757863670
geneviewrs757863670
scholarrs757863670
googlers757863670
pharmgkbrs757863670
gwascentralrs757863670
openSNPrs757863670
23andMers757863670
23andMe allrs757863670
SNP Nexus

SNPshotrs757863670
SNPdbers757863670
MSV3drs757863670
GWAS Ctlgrs757863670
Max Magnitude0
ClinVar
Risk rs757863670(G;G)
Alt rs757863670(G;G)
Reference rs757863670(A;A)
Significance Pathogenic
Disease Joubert syndrome
Variation info
Gene B9D2 TMEM91
CLNDBN Joubert syndrome
Reversed 0
HGVS NC_000019.9:g.41863909A>G
CLNSRC
CLNACC RCV000201607.1,