Rs104894903

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894903(C;T)
Make rs104894903(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position152850418
GeneNSDHL
is asnp
is mentioned by
dbSNPrs104894903
Exacrs104894903
PheGenIrs104894903
nextbiors104894903
hapmaprs104894903
1000 genomesrs104894903
hgdprs104894903
ensemblrs104894903
gopubmedrs104894903
geneviewrs104894903
scholarrs104894903
googlers104894903
pharmgkbrs104894903
gwascentralrs104894903
openSNPrs104894903
23andMers104894903
23andMe allrs104894903
SNP Nexus

SNPshotrs104894903
SNPdbers104894903
MSV3drs104894903
Max Magnitude0
OMIM300275
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894903(T;T)
Alt rs104894903(T;T)
Reference rs104894903(C;C)
Significance Pathogenic
Disease Child syndrome
Variation info
Gene NSDHL
CLNDBN Child syndrome
Reversed 0
HGVS NC_000023.10:g.152018962C>T
CLNSRC GeneReviews OMIM Allelic Variant
CLNACC RCV000012182.11,