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rs1060499784

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499784(A;A)
Make rs1060499784(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154930646
GeneF8
is asnp
is mentioned by
dbSNPrs1060499784
dbSNP (old)rs1060499784
ClinGenrs1060499784
ebirs1060499784
HLIrs1060499784
Exacrs1060499784
Gnomadrs1060499784
Varsomers1060499784
Maprs1060499784
PheGenIrs1060499784
Biobankrs1060499784
1000 genomesrs1060499784
hgdprs1060499784
ensemblrs1060499784
gopubmedrs1060499784
geneviewrs1060499784
scholarrs1060499784
googlers1060499784
pharmgkbrs1060499784
gwascentralrs1060499784
openSNPrs1060499784
23andMers1060499784
23andMe allrs1060499784
SNPshotrs1060499784
SNPdbers1060499784
MSV3drs1060499784
GWAS Ctlgrs1060499784
Max Magnitude0
ClinVar
Risk rs1060499784(A;A)
Alt rs1060499784(A;A)
Reference Rs1060499784(G;G)
Significance Probable-Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154158921C>T
CLNSRC
CLNACC RCV000454124.1,