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rs137852250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852250(C;T)
Make rs137852250(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561577
GeneF9
is asnp
is mentioned by
dbSNPrs137852250
ebirs137852250
HLIrs137852250
Exacrs137852250
Varsomers137852250
Maprs137852250
PheGenIrs137852250
hapmaprs137852250
1000 genomesrs137852250
hgdprs137852250
ensemblrs137852250
gopubmedrs137852250
geneviewrs137852250
scholarrs137852250
googlers137852250
pharmgkbrs137852250
gwascentralrs137852250
openSNPrs137852250
23andMers137852250
23andMe allrs137852250
SNP Nexus

SNPshotrs137852250
SNPdbers137852250
MSV3drs137852250
GWAS Ctlgrs137852250
Max Magnitude0
OMIM300746
Desc
Variant0046
Relatedalso
ClinVar
Risk rs137852250(T;T)
Alt rs137852250(T;T)
Reference rs137852250(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.138643736C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011349.2,