Rs104894776

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Orientationplus
is asnp
is mentioned by
dbSNPrs104894776
PheGenIrs104894776
nextbiors104894776
hapmaprs104894776
1000 genomesrs104894776
hgdprs104894776
ensemblrs104894776
gopubmedrs104894776
geneviewrs104894776
scholarrs104894776
googlers104894776
pharmgkbrs104894776
gwascentralrs104894776
openSNPrs104894776
23andMers104894776
23andMe allrs104894776
SNP Nexus

SNPshotrs104894776
SNPdbers104894776
MSV3drs104894776
GeneCD40LG
ChromosomeX
Orientationplus
Position135741208
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894776(A;A)
Make rs104894776(A;G)
OMIM300386
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104894776(A;A)
Alt rs104894776(A;A)
Reference rs104894776(G;G)
Significance 1
Disease Immunodeficiency with hyper IgM type 1
ClinVar info
Gene CD40LG
CLNDBN Immunodeficiency with hyper IgM type 1
Reversed 0
CLNHGVS NC_000023.10:g.135741208G>A
CLNSRC OMIM Allelic Variant
CLNACC SCV000032146.1, SCV000032146.1