Rs104893894

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Orientationplus
is asnp
is mentioned by
dbSNPrs104893894
PheGenIrs104893894
nextbiors104893894
hapmaprs104893894
1000 genomesrs104893894
hgdprs104893894
ensemblrs104893894
gopubmedrs104893894
geneviewrs104893894
scholarrs104893894
googlers104893894
pharmgkbrs104893894
gwascentralrs104893894
openSNPrs104893894
23andMers104893894
23andMe allrs104893894
SNP Nexus

SNPshotrs104893894
SNPdbers104893894
MSV3drs104893894
GeneIL7R
Chromosome5
Orientationplus
Position35871172
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893894(C;T)
Make rs104893894(T;T)
OMIM146661
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104893894(T;T)
Alt rs104893894(T;T)
Reference rs104893894(C;C)
Significance 5
Disease Severe combined immunodeficiency
ClinVar info
Gene IL7R
CLNDBN Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive
Reversed 0
CLNHGVS NC_000005.9:g.35871172C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015968.20