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rs200971081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200971081(A;A)
Make rs200971081(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position94368132
GeneCEP83
is asnp
is mentioned by
dbSNPrs200971081
dbSNP (classic)rs200971081
ClinGenrs200971081
ebirs200971081
HLIrs200971081
Exacrs200971081
Gnomadrs200971081
Varsomers200971081
LitVarrs200971081
Maprs200971081
PheGenIrs200971081
Biobankrs200971081
1000 genomesrs200971081
hgdprs200971081
ensemblrs200971081
geneviewrs200971081
scholarrs200971081
googlers200971081
pharmgkbrs200971081
gwascentralrs200971081
openSNPrs200971081
23andMers200971081
23andMe allrs200971081
SNPshotrs200971081
SNPdbers200971081
MSV3drs200971081
GWAS Ctlgrs200971081
Max Magnitude0
ClinVar
Risk rs200971081(A;A)
Alt rs200971081(A;A)
Reference Rs200971081(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP83 CCDC41
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.94761908T>A
CLNSRC
CLNACC RCV000434526.1,