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rs869312905

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312905(C;T)
Make rs869312905(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position225422217
GeneLBR
is asnp
is mentioned by
dbSNPrs869312905
ebirs869312905
HLIrs869312905
Exacrs869312905
Varsomers869312905
Maprs869312905
PheGenIrs869312905
hapmaprs869312905
1000 genomesrs869312905
hgdprs869312905
ensemblrs869312905
gopubmedrs869312905
geneviewrs869312905
scholarrs869312905
googlers869312905
pharmgkbrs869312905
gwascentralrs869312905
openSNPrs869312905
23andMers869312905
23andMe allrs869312905
SNP Nexus

SNPshotrs869312905
SNPdbers869312905
MSV3drs869312905
GWAS Ctlgrs869312905
Max Magnitude0
ClinVar
Risk rs869312905(T;T)
Alt rs869312905(T;T)
Reference rs869312905(C;C)
Significance Pathogenic
Disease Anadysplasia-like
Variation info
Gene LBR
CLNDBN Anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia
Reversed 1
HGVS NC_000001.10:g.225609919G>A
CLNSRC
CLNACC RCV000210455.1,