Have questions? Visit https://www.reddit.com/r/SNPedia

rs28935499

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 5.5 Hemophilia A (severity varies)
(A;G) 3.5 Carrier of a Hemophilia A mutation
(C;C) 0
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966525
GeneF8
is asnp
is mentioned by
dbSNPrs28935499
dbSNP (classic)rs28935499
ClinGenrs28935499
ebirs28935499
HLIrs28935499
Exacrs28935499
Gnomadrs28935499
Varsomers28935499
LitVarrs28935499
Maprs28935499
PheGenIrs28935499
Biobankrs28935499
1000 genomesrs28935499
hgdprs28935499
ensemblrs28935499
geneviewrs28935499
scholarrs28935499
googlers28935499
pharmgkbrs28935499
gwascentralrs28935499
openSNPrs28935499
23andMers28935499
SNPshotrs28935499
SNPdbers28935499
MSV3drs28935499
GWAS Ctlgrs28935499
Max Magnitude5.5
OMIM306700
DescFACTOR VIII (OKAYAMA)
Variant0027
Relatedalso


ClinVar
Risk Rs28935499(A;A)
Alt Rs28935499(A;A)
Reference Rs28935499(G;G)
Significance Pathogenic
Disease FACTOR VIII (OKAYAMA)
Variation info
Gene F8
CLNDBN FACTOR VIII (OKAYAMA)
Reversed 1
HGVS NC_000023.10:g.154194800C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000010823.6,