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rs863225213

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225213(A;G)
Make rs863225213(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position13736515
GeneOFD1, TRAPPC2
is asnp
is mentioned by
dbSNPrs863225213
ebirs863225213
HLIrs863225213
Exacrs863225213
Varsomers863225213
Maprs863225213
PheGenIrs863225213
hapmaprs863225213
1000 genomesrs863225213
hgdprs863225213
ensemblrs863225213
gopubmedrs863225213
geneviewrs863225213
scholarrs863225213
googlers863225213
pharmgkbrs863225213
gwascentralrs863225213
openSNPrs863225213
23andMers863225213
23andMe allrs863225213
SNP Nexus

SNPshotrs863225213
SNPdbers863225213
MSV3drs863225213
GWAS Ctlgrs863225213
Max Magnitude0
ClinVar
Risk rs863225213(G;G)
Alt rs863225213(G;G)
Reference rs863225213(A;A)
Significance Pathogenic
Disease Joubert syndrome 10
Variation info
Gene TRAPPC2 OFD1
CLNDBN Joubert syndrome 10
Reversed 0
HGVS NC_000023.10:g.13754634A>G
CLNSRC
CLNACC RCV000201618.1,