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rs879254290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs879254290(-;C)
Make rs879254290(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome8
Position133250456
GeneNDRG1
is asnp
is mentioned by
dbSNPrs879254290
dbSNP (classic)rs879254290
ClinGenrs879254290
ebirs879254290
HLIrs879254290
Exacrs879254290
Gnomadrs879254290
Varsomers879254290
LitVarrs879254290
Maprs879254290
PheGenIrs879254290
Biobankrs879254290
1000 genomesrs879254290
hgdprs879254290
ensemblrs879254290
geneviewrs879254290
scholarrs879254290
googlers879254290
pharmgkbrs879254290
gwascentralrs879254290
openSNPrs879254290
23andMers879254290
SNPshotrs879254290
SNPdbers879254290
MSV3drs879254290
GWAS Ctlgrs879254290
Max Magnitude0
ClinVar
Risk rs879254290(C;C)
Alt rs879254290(C;C)
Reference Rs879254290(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene NDRG1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.134262700dupG
CLNSRC
CLNACC RCV000236853.2,