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rs119490107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs119490107(G;T)
Make rs119490107(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position94399540
GeneRAD54B
is asnp
is mentioned by
dbSNPrs119490107
ebirs119490107
HLIrs119490107
Exacrs119490107
Varsomers119490107
Maprs119490107
PheGenIrs119490107
hapmaprs119490107
1000 genomesrs119490107
hgdprs119490107
ensemblrs119490107
gopubmedrs119490107
geneviewrs119490107
scholarrs119490107
googlers119490107
pharmgkbrs119490107
gwascentralrs119490107
openSNPrs119490107
23andMers119490107
23andMe allrs119490107
SNP Nexus

SNPshotrs119490107
SNPdbers119490107
MSV3drs119490107
GWAS Ctlgrs119490107
Max Magnitude0
OMIM604289
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119490107(T;T)
Alt rs119490107(T;T)
Reference rs119490107(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene RAD54B
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000008.10:g.95411768C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005993.6,