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

rs374426474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374426474(C;T)
Make rs374426474(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position86716734
GeneLDB3
is asnp
is mentioned by
dbSNPrs374426474
dbSNP (classic)rs374426474
ClinGenrs374426474
ebirs374426474
HLIrs374426474
Exacrs374426474
Gnomadrs374426474
Varsomers374426474
LitVarrs374426474
Maprs374426474
PheGenIrs374426474
Biobankrs374426474
1000 genomesrs374426474
hgdprs374426474
ensemblrs374426474
geneviewrs374426474
scholarrs374426474
googlers374426474
pharmgkbrs374426474
gwascentralrs374426474
openSNPrs374426474
23andMers374426474
SNPshotrs374426474
SNPdbers374426474
MSV3drs374426474
GWAS Ctlgrs374426474
Max Magnitude0
ClinVar
Risk rs374426474(T;T)
Alt rs374426474(T;T)
Reference Rs374426474(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene LDB3
CLNDBN not specified
Reversed 0
HGVS NC_000010.10:g.88476491C>T
CLNSRC
CLNACC RCV000183540.2,