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rs777854951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777854951(G;T)
Make rs777854951(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position21741710
GeneMIB1
is asnp
is mentioned by
dbSNPrs777854951
dbSNP (classic)rs777854951
ClinGenrs777854951
ebirs777854951
HLIrs777854951
Exacrs777854951
Gnomadrs777854951
Varsomers777854951
LitVarrs777854951
Maprs777854951
PheGenIrs777854951
Biobankrs777854951
1000 genomesrs777854951
hgdprs777854951
ensemblrs777854951
geneviewrs777854951
scholarrs777854951
googlers777854951
pharmgkbrs777854951
gwascentralrs777854951
openSNPrs777854951
23andMers777854951
23andMe allrs777854951
SNPshotrs777854951
SNPdbers777854951
MSV3drs777854951
GWAS Ctlgrs777854951
Max Magnitude0
ClinVar
Risk rs777854951(T;T)
Alt rs777854951(T;T)
Reference Rs777854951(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIB1
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.19321671G>T
CLNSRC
CLNACC RCV000432654.1,