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rs374343844

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs374343844(A;A)
Make rs374343844(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position225404451
GeneLBR
is asnp
is mentioned by
dbSNPrs374343844
ebirs374343844
HLIrs374343844
Exacrs374343844
Varsomers374343844
Maprs374343844
PheGenIrs374343844
hapmaprs374343844
1000 genomesrs374343844
hgdprs374343844
ensemblrs374343844
gopubmedrs374343844
geneviewrs374343844
scholarrs374343844
googlers374343844
pharmgkbrs374343844
gwascentralrs374343844
openSNPrs374343844
23andMers374343844
23andMe allrs374343844
SNP Nexus

SNPshotrs374343844
SNPdbers374343844
MSV3drs374343844
GWAS Ctlgrs374343844
Max Magnitude0
ClinVar
Risk rs374343844(A,C;A,C)
Alt rs374343844(A,C;A,C)
Reference rs374343844(T;T)
Significance Pathogenic
Disease Anadysplasia-like
Variation info
Gene LBR
CLNDBN Anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia
Reversed 0
HGVS NC_000001.10:g.225592153T>C
CLNSRC
CLNACC RCV000210471.1,