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rs114216685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs114216685(C;C)
Make rs114216685(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position94391640
GeneRAD54B
is asnp
is mentioned by
dbSNPrs114216685
ebirs114216685
HLIrs114216685
Exacrs114216685
Varsomers114216685
Maprs114216685
PheGenIrs114216685
hapmaprs114216685
1000 genomesrs114216685
hgdprs114216685
ensemblrs114216685
gopubmedrs114216685
geneviewrs114216685
scholarrs114216685
googlers114216685
pharmgkbrs114216685
gwascentralrs114216685
openSNPrs114216685
23andMers114216685
23andMe allrs114216685
SNP Nexus

SNPshotrs114216685
SNPdbers114216685
MSV3drs114216685
GWAS Ctlgrs114216685
GMAF0.004132
Max Magnitude0
OMIM604289
Desc
Variant0001
Relatedalso
ClinVar
Risk rs114216685(C;C)
Alt rs114216685(C;C)
Reference rs114216685(T;T)
Significance Pathogenic
Disease Malignant lymphoma
Variation info
Gene RAD54B
CLNDBN Malignant lymphoma, non-Hodgkin
Reversed 0
HGVS NC_000008.10:g.95403868T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005992.6,