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rs138269726

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138269726(C;T)
Make rs138269726(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position169212088
GeneLRP2
is asnp
is mentioned by
dbSNPrs138269726
ebirs138269726
HLIrs138269726
Exacrs138269726
Varsomers138269726
Maprs138269726
PheGenIrs138269726
hapmaprs138269726
1000 genomesrs138269726
hgdprs138269726
ensemblrs138269726
gopubmedrs138269726
geneviewrs138269726
scholarrs138269726
googlers138269726
pharmgkbrs138269726
gwascentralrs138269726
openSNPrs138269726
23andMers138269726
23andMe allrs138269726
SNP Nexus

SNPshotrs138269726
SNPdbers138269726
MSV3drs138269726
GWAS Ctlgrs138269726
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs138269726(T;T)
Alt rs138269726(T;T)
Reference rs138269726(C;C)
Significance Pathogenic
Disease Donnai Barrow syndrome
Variation info
Gene LRP2
CLNDBN Donnai Barrow syndrome
Reversed 0
HGVS NC_000002.11:g.170068598C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033108.4,