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rs875989884

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989884(C;T)
Make rs875989884(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153866700
GeneL1CAM
is asnp
is mentioned by
dbSNPrs875989884
ebirs875989884
HLIrs875989884
Exacrs875989884
Varsomers875989884
Maprs875989884
PheGenIrs875989884
hapmaprs875989884
1000 genomesrs875989884
hgdprs875989884
ensemblrs875989884
gopubmedrs875989884
geneviewrs875989884
scholarrs875989884
googlers875989884
pharmgkbrs875989884
gwascentralrs875989884
openSNPrs875989884
23andMers875989884
23andMe allrs875989884
SNP Nexus

SNPshotrs875989884
SNPdbers875989884
MSV3drs875989884
GWAS Ctlgrs875989884
Max Magnitude0
ClinVar
Risk rs875989884(T;T)
Alt rs875989884(T;T)
Reference rs875989884(C;C)
Significance Pathogenic
Disease X-linked hydrocephalus syndrome
Variation info
Gene L1CAM
CLNDBN X-linked hydrocephalus syndrome
Reversed 1
HGVS NC_000023.10:g.153132155G>A
CLNSRC University Hospital of Geneva
CLNACC RCV000211546.1,