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rs121908690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908690(A;A)
Make rs121908690(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position46267540
GeneRAD54L
is asnp
is mentioned by
dbSNPrs121908690
ebirs121908690
HLIrs121908690
Exacrs121908690
Varsomers121908690
Maprs121908690
PheGenIrs121908690
hapmaprs121908690
1000 genomesrs121908690
hgdprs121908690
ensemblrs121908690
gopubmedrs121908690
geneviewrs121908690
scholarrs121908690
googlers121908690
pharmgkbrs121908690
gwascentralrs121908690
openSNPrs121908690
23andMers121908690
23andMe allrs121908690
SNP Nexus

SNPshotrs121908690
SNPdbers121908690
MSV3drs121908690
GWAS Ctlgrs121908690
Max Magnitude0
OMIM603615
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908690(A;A)
Alt rs121908690(A;A)
Reference rs121908690(G;G)
Significance Pathogenic
Disease Ductal breast carcinoma
Variation info
Gene RAD54L
CLNDBN Ductal breast carcinoma
Reversed 0
HGVS NC_000001.10:g.46733212G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006570.2,