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

rs137852249

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852249(A;A)
Make rs137852249(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561566
GeneF9
is asnp
is mentioned by
dbSNPrs137852249
ebirs137852249
HLIrs137852249
Exacrs137852249
Varsomers137852249
Maprs137852249
PheGenIrs137852249
hapmaprs137852249
1000 genomesrs137852249
hgdprs137852249
ensemblrs137852249
gopubmedrs137852249
geneviewrs137852249
scholarrs137852249
googlers137852249
pharmgkbrs137852249
gwascentralrs137852249
openSNPrs137852249
23andMers137852249
23andMe allrs137852249
SNP Nexus

SNPshotrs137852249
SNPdbers137852249
MSV3drs137852249
GWAS Ctlgrs137852249
Max Magnitude0
OMIM300746
Desc
Variant0045
Relatedalso
ClinVar
Risk rs137852249(A;A)
Alt rs137852249(A;A)
Reference rs137852249(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.138643725G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011348.7,