Rs104894902

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894902(C;T)
Make rs104894902(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position152865903
GeneNSDHL
is asnp
is mentioned by
dbSNPrs104894902
Exacrs104894902
PheGenIrs104894902
nextbiors104894902
hapmaprs104894902
1000 genomesrs104894902
hgdprs104894902
ensemblrs104894902
gopubmedrs104894902
geneviewrs104894902
scholarrs104894902
googlers104894902
pharmgkbrs104894902
gwascentralrs104894902
openSNPrs104894902
23andMers104894902
23andMe allrs104894902
SNP Nexus

SNPshotrs104894902
SNPdbers104894902
MSV3drs104894902
Max Magnitude0
OMIM300275
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894902(T;T)
Alt rs104894902(T;T)
Reference rs104894902(C;C)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152034447C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012181.10,