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rs121908689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs121908689(A;A)
Make rs121908689(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position46272758
GeneRAD54L
is asnp
is mentioned by
dbSNPrs121908689
ebirs121908689
HLIrs121908689
Exacrs121908689
Varsomers121908689
Maprs121908689
PheGenIrs121908689
hapmaprs121908689
1000 genomesrs121908689
hgdprs121908689
ensemblrs121908689
gopubmedrs121908689
geneviewrs121908689
scholarrs121908689
googlers121908689
pharmgkbrs121908689
gwascentralrs121908689
openSNPrs121908689
23andMers121908689
23andMe allrs121908689
SNP Nexus

SNPshotrs121908689
SNPdbers121908689
MSV3drs121908689
GWAS Ctlgrs121908689
Max Magnitude0
OMIM603615
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908689(A;A)
Alt rs121908689(A;A)
Reference rs121908689(T;T)
Significance Pathogenic
Disease Malignant lymphoma
Variation info
Gene RAD54L
CLNDBN Malignant lymphoma, non-Hodgkin
Reversed 0
HGVS NC_000001.10:g.46738430T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006569.4,