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rs267606792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606792(C;C)
Make rs267606792(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139560772
GeneF9
is asnp
is mentioned by
dbSNPrs267606792
ebirs267606792
HLIrs267606792
Exacrs267606792
Varsomers267606792
Maprs267606792
PheGenIrs267606792
hapmaprs267606792
1000 genomesrs267606792
hgdprs267606792
ensemblrs267606792
gopubmedrs267606792
geneviewrs267606792
scholarrs267606792
googlers267606792
pharmgkbrs267606792
gwascentralrs267606792
openSNPrs267606792
23andMers267606792
23andMe allrs267606792
SNP Nexus

SNPshotrs267606792
SNPdbers267606792
MSV3drs267606792
GWAS Ctlgrs267606792
Max Magnitude0
ClinVar
Risk rs267606792(C;C)
Alt rs267606792(C;C)
Reference rs267606792(G;G)
Significance Pathogenic
Disease Hereditary factor IX deficiency disease
Variation info
Gene F9
CLNDBN Hereditary factor IX deficiency disease
Reversed 0
HGVS NC_000023.10:g.138642931G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011411.3,