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

rs772174079

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772174079(A;A)
Make rs772174079(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50222507
GeneTUBGCP6
is asnp
is mentioned by
dbSNPrs772174079
ebirs772174079
HLIrs772174079
Exacrs772174079
Varsomers772174079
Maprs772174079
PheGenIrs772174079
hapmaprs772174079
1000 genomesrs772174079
hgdprs772174079
ensemblrs772174079
gopubmedrs772174079
geneviewrs772174079
scholarrs772174079
googlers772174079
pharmgkbrs772174079
gwascentralrs772174079
openSNPrs772174079
23andMers772174079
23andMe allrs772174079
SNP Nexus

SNPshotrs772174079
SNPdbers772174079
MSV3drs772174079
GWAS Ctlgrs772174079
Max Magnitude0
ClinVar
Risk rs772174079(A,T;A,T)
Alt rs772174079(A,T;A,T)
Reference rs772174079(G;G)
Significance Pathogenic
Disease Microcephaly and chorioretinopathy with or without mental retardation
Variation info
Gene TUBGCP6
CLNDBN Microcephaly and chorioretinopathy with or without mental retardation
Reversed 0
HGVS NC_000022.10:g.50660936G>A
CLNSRC
CLNACC RCV000194400.1,