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rs797045673

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045673(C;T)
Make rs797045673(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153866802
GeneL1CAM
is asnp
is mentioned by
dbSNPrs797045673
ebirs797045673
HLIrs797045673
Exacrs797045673
Varsomers797045673
Maprs797045673
PheGenIrs797045673
hapmaprs797045673
1000 genomesrs797045673
hgdprs797045673
ensemblrs797045673
gopubmedrs797045673
geneviewrs797045673
scholarrs797045673
googlers797045673
pharmgkbrs797045673
gwascentralrs797045673
openSNPrs797045673
23andMers797045673
23andMe allrs797045673
SNP Nexus

SNPshotrs797045673
SNPdbers797045673
MSV3drs797045673
GWAS Ctlgrs797045673
Max Magnitude0
ClinVar
Risk rs797045673(T;T)
Alt rs797045673(T;T)
Reference rs797045673(C;C)
Significance Pathogenic
Disease Hydrocephalus due to aqueductal stenosis
Variation info
Gene L1CAM
CLNDBN Hydrocephalus due to aqueductal stenosis
Reversed 1
HGVS NC_000023.10:g.153132257G>A
CLNSRC
CLNACC RCV000193744.1,