Rs104894183

From SNPedia
Jump to: navigation, search

Orientationminus
is asnp
is mentioned by
dbSNPrs104894183
PheGenIrs104894183
nextbiors104894183
hapmaprs104894183
1000 genomesrs104894183
hgdprs104894183
ensemblrs104894183
gopubmedrs104894183
geneviewrs104894183
scholarrs104894183
googlers104894183
pharmgkbrs104894183
gwascentralrs104894183
openSNPrs104894183
23andMers104894183
23andMe allrs104894183
SNP Nexus

SNPshotrs104894183
SNPdbers104894183
MSV3drs104894183
GenePRF1
Chromosome10
Orientationminus
Position72358929
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894183(G;G)
Make rs104894183(G;T)
OMIM170280
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894183(G;G)
Alt rs104894183(G;G)
Reference rs104894183(T;T)
Significance 5
Disease Hemophagocytic lymphohistiocytosis
ClinVar info
Gene PRF1
CLNDBN Hemophagocytic lymphohistiocytosis, familial, 2
Reversed 1
CLNHGVS NC_000010.10:g.72358929A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014715.21