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rs28935499

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28935499(A;A)
Make rs28935499(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966525
GeneF8
is asnp
is mentioned by
dbSNPrs28935499
ebirs28935499
HLIrs28935499
Exacrs28935499
Varsomers28935499
Maprs28935499
PheGenIrs28935499
hapmaprs28935499
1000 genomesrs28935499
hgdprs28935499
ensemblrs28935499
gopubmedrs28935499
geneviewrs28935499
scholarrs28935499
googlers28935499
pharmgkbrs28935499
gwascentralrs28935499
openSNPrs28935499
23andMers28935499
23andMe allrs28935499
SNP Nexus

SNPshotrs28935499
SNPdbers28935499
MSV3drs28935499
GWAS Ctlgrs28935499
Max Magnitude0
OMIM306700
DescFACTOR VIII (OKAYAMA)
Variant0027
Relatedalso
Neighborrs28933669
Distance2


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
CLNACC RCV000010823.6,