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

rs137852224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852224(C;C)
Make rs137852224(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139537111
GeneF9
is asnp
is mentioned by
dbSNPrs137852224
ebirs137852224
HLIrs137852224
Exacrs137852224
Varsomers137852224
Maprs137852224
PheGenIrs137852224
hapmaprs137852224
1000 genomesrs137852224
hgdprs137852224
ensemblrs137852224
gopubmedrs137852224
geneviewrs137852224
scholarrs137852224
googlers137852224
pharmgkbrs137852224
gwascentralrs137852224
openSNPrs137852224
23andMers137852224
23andMe allrs137852224
SNP Nexus

SNPshotrs137852224
SNPdbers137852224
MSV3drs137852224
GWAS Ctlgrs137852224
Max Magnitude0
OMIM300746
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137852224(C;C)
Alt rs137852224(C;C)
Reference rs137852224(T;T)
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.138619270T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011314.6,