Rs104894807

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Orientationplus
Geno Mag Summary
(C;T) 3 hemophilia B if male; carrier if female
(T;T) 0 common in clinvar


Make rs104894807(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139548404
GeneF9
is asnp
is mentioned by
dbSNPrs104894807
Exacrs104894807
PheGenIrs104894807
nextbiors104894807
hapmaprs104894807
1000 genomesrs104894807
hgdprs104894807
ensemblrs104894807
gopubmedrs104894807
geneviewrs104894807
scholarrs104894807
googlers104894807
pharmgkbrs104894807
gwascentralrs104894807
openSNPrs104894807
23andMers104894807
23andMe allrs104894807
SNP Nexus

SNPshotrs104894807
SNPdbers104894807
MSV3drs104894807
OMIM300746
Desc
Variant0026
Relatedalso
ClinVar
Risk rs104894807(C;C)
Alt rs104894807(C;C)
Reference rs104894807(T;T)
Significance Untested
Disease
Variation info
Gene F9
CLNDBN
Reversed 0
HGVS NC_000023.10:g.138630563T>C
CLNSRC
CLNACC