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rs879255267

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255267(G;T)
Make rs879255267(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position107975026
GeneLAMB1
is asnp
is mentioned by
dbSNPrs879255267
ebirs879255267
HLIrs879255267
Exacrs879255267
Varsomers879255267
Maprs879255267
PheGenIrs879255267
hapmaprs879255267
1000 genomesrs879255267
hgdprs879255267
ensemblrs879255267
gopubmedrs879255267
geneviewrs879255267
scholarrs879255267
googlers879255267
pharmgkbrs879255267
gwascentralrs879255267
openSNPrs879255267
23andMers879255267
23andMe allrs879255267
SNP Nexus

SNPshotrs879255267
SNPdbers879255267
MSV3drs879255267
GWAS Ctlgrs879255267
Max Magnitude0
ClinVar
Risk rs879255267(T;T)
Alt rs879255267(T;T)
Reference rs879255267(G;G)
Significance Pathogenic
Disease Lissencephaly 5
Variation info
Gene LAMB1
CLNDBN Lissencephaly 5
Reversed 1
HGVS NC_000007.13:g.107615471C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210961.1,