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rs797044787

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044787(C;T)
Make rs797044787(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position153870123
GeneL1CAM
is asnp
is mentioned by
dbSNPrs797044787
ebirs797044787
HLIrs797044787
Exacrs797044787
Varsomers797044787
Maprs797044787
PheGenIrs797044787
hapmaprs797044787
1000 genomesrs797044787
hgdprs797044787
ensemblrs797044787
gopubmedrs797044787
geneviewrs797044787
scholarrs797044787
googlers797044787
pharmgkbrs797044787
gwascentralrs797044787
openSNPrs797044787
23andMers797044787
23andMe allrs797044787
SNP Nexus

SNPshotrs797044787
SNPdbers797044787
MSV3drs797044787
GWAS Ctlgrs797044787
Max Magnitude0
ClinVar
Risk rs797044787(T;T)
Alt rs797044787(T;T)
Reference rs797044787(C;C)
Significance Other
Disease X-linked hydrocephalus syndrome
Variation info
Gene L1CAM
CLNDBN X-linked hydrocephalus syndrome
Reversed 1
HGVS NC_000023.10:g.153135578G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000180160.2,