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rs778947880

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778947880(C;T)
Make rs778947880(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position21765807
GeneMIB1
is asnp
is mentioned by
dbSNPrs778947880
dbSNP (old)rs778947880
ClinGenrs778947880
ebirs778947880
HLIrs778947880
Exacrs778947880
Gnomadrs778947880
Varsomers778947880
Maprs778947880
PheGenIrs778947880
Biobankrs778947880
1000 genomesrs778947880
hgdprs778947880
ensemblrs778947880
gopubmedrs778947880
geneviewrs778947880
scholarrs778947880
googlers778947880
pharmgkbrs778947880
gwascentralrs778947880
openSNPrs778947880
23andMers778947880
23andMe allrs778947880
SNPshotrs778947880
SNPdbers778947880
MSV3drs778947880
GWAS Ctlgrs778947880
Max Magnitude0
ClinVar
Risk rs778947880(G;G) rs778947880(T;T)
Alt rs778947880(G;G) rs778947880(T;T)
Reference Rs778947880(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIB1
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.19345768C>T
CLNSRC
CLNACC RCV000481876.1,