Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121908688(A;A)
Make rs121908688(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position46250097
GeneRAD54L
is asnp
is mentioned by
dbSNPrs121908688
ebirs121908688
HLIrs121908688
Exacrs121908688
Varsomers121908688
Maprs121908688
PheGenIrs121908688
hapmaprs121908688
1000 genomesrs121908688
hgdprs121908688
ensemblrs121908688
gopubmedrs121908688
geneviewrs121908688
scholarrs121908688
googlers121908688
pharmgkbrs121908688
gwascentralrs121908688
openSNPrs121908688
23andMers121908688
23andMe allrs121908688
SNP Nexus

SNPshotrs121908688
SNPdbers121908688
MSV3drs121908688
GWAS Ctlgrs121908688
Max Magnitude0
OMIM603615
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908688(A;A)
Alt rs121908688(A;A)
Reference rs121908688(C;C)
Significance Pathogenic
Disease Colonic adenocarcinoma
Variation info
Gene RAD54L
CLNDBN Colonic adenocarcinoma
Reversed 0
HGVS NC_000001.10:g.46715769C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006568.4,