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rs755459875

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs755459875(G;G)
Make rs755459875(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position61397942
GeneTMEM216
is asnp
is mentioned by
dbSNPrs755459875
ebirs755459875
HLIrs755459875
Exacrs755459875
Varsomers755459875
Maprs755459875
PheGenIrs755459875
hapmaprs755459875
1000 genomesrs755459875
hgdprs755459875
ensemblrs755459875
gopubmedrs755459875
geneviewrs755459875
scholarrs755459875
googlers755459875
pharmgkbrs755459875
gwascentralrs755459875
openSNPrs755459875
23andMers755459875
23andMe allrs755459875
SNP Nexus

SNPshotrs755459875
SNPdbers755459875
MSV3drs755459875
GWAS Ctlgrs755459875
Max Magnitude0
ClinVar
Risk rs755459875(G;G)
Alt rs755459875(G;G)
Reference rs755459875(T;T)
Significance Pathogenic
Disease Joubert syndrome 2
Variation info
Gene TMEM216
CLNDBN Joubert syndrome 2
Reversed 0
HGVS NC_000011.9:g.61165414T>G
CLNSRC
CLNACC RCV000201555.1,