Rs104894176

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894176(A;A)
Make rs104894176(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position70598599
GenePRF1
is asnp
is mentioned by
dbSNPrs104894176
Exacrs104894176
PheGenIrs104894176
nextbiors104894176
hapmaprs104894176
1000 genomesrs104894176
hgdprs104894176
ensemblrs104894176
gopubmedrs104894176
geneviewrs104894176
scholarrs104894176
googlers104894176
pharmgkbrs104894176
gwascentralrs104894176
openSNPrs104894176
23andMers104894176
23andMe allrs104894176
SNP Nexus

SNPshotrs104894176
SNPdbers104894176
MSV3drs104894176
Max Magnitude0
OMIM170280
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894176(A;A)
Alt rs104894176(A;A)
Reference rs104894176(G;G)
Significance Pathogenic
Disease Hemophagocytic lymphohistiocytosis Malignant lymphoma
Variation info
Gene PRF1
CLNDBN Hemophagocytic lymphohistiocytosis, familial, 2 Malignant lymphoma, non-Hodgkin
Reversed 1
HGVS NC_000010.10:g.72358355C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014708.24, RCV000014709.21,