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rs121908982

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121908982(C;T)
Make rs121908982(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position2225526
GeneMAD1L1
is asnp
is mentioned by
dbSNPrs121908982
ebirs121908982
HLIrs121908982
Exacrs121908982
Varsomers121908982
Maprs121908982
PheGenIrs121908982
hapmaprs121908982
1000 genomesrs121908982
hgdprs121908982
ensemblrs121908982
gopubmedrs121908982
geneviewrs121908982
scholarrs121908982
googlers121908982
pharmgkbrs121908982
gwascentralrs121908982
openSNPrs121908982
23andMers121908982
23andMe allrs121908982
SNP Nexus

SNPshotrs121908982
SNPdbers121908982
MSV3drs121908982
GWAS Ctlgrs121908982
Merged fromRs28939694
GMAF0.0009183
Max Magnitude0
OMIM602686
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908982(T;T)
Alt rs121908982(T;T)
Reference Rs121908982(C;C)
Significance Pathogenic
Disease Prostate cancer
Variation info
Gene MAD1L1
CLNDBN Prostate cancer, somatic
Reversed 1
HGVS NC_000007.13:g.2265161G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000007329.4,