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

rs137852263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852263(C;T)
Make rs137852263(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561902
GeneF9
is asnp
is mentioned by
dbSNPrs137852263
ebirs137852263
HLIrs137852263
Exacrs137852263
Varsomers137852263
Maprs137852263
PheGenIrs137852263
hapmaprs137852263
1000 genomesrs137852263
hgdprs137852263
ensemblrs137852263
gopubmedrs137852263
geneviewrs137852263
scholarrs137852263
googlers137852263
pharmgkbrs137852263
gwascentralrs137852263
openSNPrs137852263
23andMers137852263
23andMe allrs137852263
SNP Nexus

SNPshotrs137852263
SNPdbers137852263
MSV3drs137852263
GWAS Ctlgrs137852263
Max Magnitude0
OMIM300746
Desc
Variant0061
Relatedalso
ClinVar
Risk rs137852263(T;T)
Alt rs137852263(T;T)
Reference rs137852263(C;C)
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.138644061C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011363.6,