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rs267606791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606791(G;T)
Make rs267606791(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154902150
GeneF8
is asnp
is mentioned by
dbSNPrs267606791
ebirs267606791
HLIrs267606791
Exacrs267606791
Varsomers267606791
Maprs267606791
PheGenIrs267606791
hapmaprs267606791
1000 genomesrs267606791
hgdprs267606791
ensemblrs267606791
gopubmedrs267606791
geneviewrs267606791
scholarrs267606791
googlers267606791
pharmgkbrs267606791
gwascentralrs267606791
openSNPrs267606791
23andMers267606791
23andMe allrs267606791
SNP Nexus

SNPshotrs267606791
SNPdbers267606791
MSV3drs267606791
GWAS Ctlgrs267606791
Max Magnitude0
ClinVar
Risk rs267606791(T;T)
Alt rs267606791(T;T)
Reference rs267606791(G;G)
Significance Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154130425C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011016.4,