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

rs374567435

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374567435(C;T)
Make rs374567435(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position46274151
GeneRAD54L
is asnp
is mentioned by
dbSNPrs374567435
ebirs374567435
HLIrs374567435
Exacrs374567435
Varsomers374567435
Maprs374567435
PheGenIrs374567435
hapmaprs374567435
1000 genomesrs374567435
hgdprs374567435
ensemblrs374567435
gopubmedrs374567435
geneviewrs374567435
scholarrs374567435
googlers374567435
pharmgkbrs374567435
gwascentralrs374567435
openSNPrs374567435
23andMers374567435
23andMe allrs374567435
SNP Nexus

SNPshotrs374567435
SNPdbers374567435
MSV3drs374567435
GWAS Ctlgrs374567435
Max Magnitude0
ClinVar
Risk rs374567435(T;T)
Alt rs374567435(T;T)
Reference rs374567435(C;C)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RAD54L
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.46739823C>T
CLNSRC
CLNACC RCV000210737.1,