Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225211

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225211(G;T)
Make rs863225211(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position13736643
GeneOFD1
is asnp
is mentioned by
dbSNPrs863225211
ebirs863225211
HLIrs863225211
Exacrs863225211
Varsomers863225211
Maprs863225211
PheGenIrs863225211
hapmaprs863225211
1000 genomesrs863225211
hgdprs863225211
ensemblrs863225211
gopubmedrs863225211
geneviewrs863225211
scholarrs863225211
googlers863225211
pharmgkbrs863225211
gwascentralrs863225211
openSNPrs863225211
23andMers863225211
23andMe allrs863225211
SNP Nexus

SNPshotrs863225211
SNPdbers863225211
MSV3drs863225211
GWAS Ctlgrs863225211
Max Magnitude0
ClinVar
Risk rs863225211(T;T)
Alt rs863225211(T;T)
Reference rs863225211(G;G)
Significance Pathogenic
Disease Joubert syndrome 10
Variation info
Gene OFD1
CLNDBN Joubert syndrome 10
Reversed 0
HGVS NC_000023.10:g.13754762G>T
CLNSRC
CLNACC RCV000201699.1,