Rs104894181

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Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894181(A;A)
Make rs104894181(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position70598435
GenePRF1
is asnp
is mentioned by
dbSNPrs104894181
Exacrs104894181
PheGenIrs104894181
nextbiors104894181
hapmaprs104894181
1000 genomesrs104894181
hgdprs104894181
ensemblrs104894181
gopubmedrs104894181
geneviewrs104894181
scholarrs104894181
googlers104894181
pharmgkbrs104894181
gwascentralrs104894181
openSNPrs104894181
23andMers104894181
23andMe allrs104894181
SNP Nexus

SNPshotrs104894181
SNPdbers104894181
MSV3drs104894181
OMIM170280
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894181(A;A)
Alt rs104894181(A;A)
Reference rs104894181(G;G)
Significance Pathogenic
Disease Hemophagocytic lymphohistiocytosis
Variation info
Gene PRF1
CLNDBN Hemophagocytic lymphohistiocytosis, familial, 2
Reversed 1
HGVS NC_000010.10:g.72358191C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014712.24,