Rs104894771

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894771(C;C)
Make rs104894771(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136659332
GeneCD40LG
is asnp
is mentioned by
dbSNPrs104894771
Exacrs104894771
PheGenIrs104894771
nextbiors104894771
hapmaprs104894771
1000 genomesrs104894771
hgdprs104894771
ensemblrs104894771
gopubmedrs104894771
geneviewrs104894771
scholarrs104894771
googlers104894771
pharmgkbrs104894771
gwascentralrs104894771
openSNPrs104894771
23andMers104894771
23andMe allrs104894771
SNP Nexus

SNPshotrs104894771
SNPdbers104894771
MSV3drs104894771
Max Magnitude0
OMIM300386
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894771(C;C)
Alt rs104894771(C;C)
Reference rs104894771(G;G)
Significance Pathogenic
Disease Immunodeficiency with hyper IgM type 1
Variation info
Gene CD40LG
CLNDBN Immunodeficiency with hyper IgM type 1
Reversed 0
HGVS NC_000023.10:g.135741491G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011907.1,