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rs137852605

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852605(C;T)
Make rs137852605(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position225422087
GeneLBR
is asnp
is mentioned by
dbSNPrs137852605
ebirs137852605
HLIrs137852605
Exacrs137852605
Varsomers137852605
Maprs137852605
PheGenIrs137852605
hapmaprs137852605
1000 genomesrs137852605
hgdprs137852605
ensemblrs137852605
gopubmedrs137852605
geneviewrs137852605
scholarrs137852605
googlers137852605
pharmgkbrs137852605
gwascentralrs137852605
openSNPrs137852605
23andMers137852605
23andMe allrs137852605
SNP Nexus

SNPshotrs137852605
SNPdbers137852605
MSV3drs137852605
GWAS Ctlgrs137852605
Max Magnitude0
OMIM600024
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852605(T;T)
Alt rs137852605(T;T)
Reference rs137852605(C;C)
Significance Pathogenic
Disease Pelger-Huët anomaly
Variation info
Gene LBR
CLNDBN Pelger-Huët anomaly
Reversed 1
HGVS NC_000001.10:g.225609789G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010138.2,