Rs104894183

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894183(G;G)
Make rs104894183(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position70599173
GenePRF1
is asnp
is mentioned by
dbSNPrs104894183
Exacrs104894183
PheGenIrs104894183
nextbiors104894183
hapmaprs104894183
1000 genomesrs104894183
hgdprs104894183
ensemblrs104894183
gopubmedrs104894183
geneviewrs104894183
scholarrs104894183
googlers104894183
pharmgkbrs104894183
gwascentralrs104894183
openSNPrs104894183
23andMers104894183
23andMe allrs104894183
SNP Nexus

SNPshotrs104894183
SNPdbers104894183
MSV3drs104894183
Max Magnitude0
OMIM170280
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894183(G;G)
Alt rs104894183(G;G)
Reference rs104894183(T;T)
Significance Pathogenic
Disease Hemophagocytic lymphohistiocytosis
Variation info
Gene PRF1
CLNDBN Hemophagocytic lymphohistiocytosis, familial, 2
Reversed 1
HGVS NC_000010.10:g.72358929A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014715.21,