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rs775883520

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775883520(A;G)
Make rs775883520(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93780603
GeneTMEM67
is asnp
is mentioned by
dbSNPrs775883520
ebirs775883520
HLIrs775883520
Exacrs775883520
Varsomers775883520
Maprs775883520
PheGenIrs775883520
hapmaprs775883520
1000 genomesrs775883520
hgdprs775883520
ensemblrs775883520
gopubmedrs775883520
geneviewrs775883520
scholarrs775883520
googlers775883520
pharmgkbrs775883520
gwascentralrs775883520
openSNPrs775883520
23andMers775883520
23andMe allrs775883520
SNP Nexus

SNPshotrs775883520
SNPdbers775883520
MSV3drs775883520
GWAS Ctlgrs775883520
Max Magnitude0
ClinVar
Risk rs775883520(G;G)
Alt rs775883520(G;G)
Reference rs775883520(A;A)
Significance Pathogenic
Disease Familial aplasia of the vermis Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Familial aplasia of the vermis Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94792831A>G
CLNSRC
CLNACC RCV000198666.2, RCV000201726.1,