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rs797045674

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045674(A;G)
Make rs797045674(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153866729
GeneL1CAM
is asnp
is mentioned by
dbSNPrs797045674
ebirs797045674
HLIrs797045674
Exacrs797045674
Varsomers797045674
Maprs797045674
PheGenIrs797045674
hapmaprs797045674
1000 genomesrs797045674
hgdprs797045674
ensemblrs797045674
gopubmedrs797045674
geneviewrs797045674
scholarrs797045674
googlers797045674
pharmgkbrs797045674
gwascentralrs797045674
openSNPrs797045674
23andMers797045674
23andMe allrs797045674
SNP Nexus

SNPshotrs797045674
SNPdbers797045674
MSV3drs797045674
GWAS Ctlgrs797045674
Max Magnitude0
ClinVar
Risk rs797045674(G;G)
Alt rs797045674(G;G)
Reference rs797045674(A;A)
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.153132184T>C
CLNSRC
CLNACC RCV000192536.1,