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rs137852231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852231(A;C)
Make rs137852231(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139541085
GeneF9
is asnp
is mentioned by
dbSNPrs137852231
ebirs137852231
HLIrs137852231
Exacrs137852231
Varsomers137852231
Maprs137852231
PheGenIrs137852231
hapmaprs137852231
1000 genomesrs137852231
hgdprs137852231
ensemblrs137852231
gopubmedrs137852231
geneviewrs137852231
scholarrs137852231
googlers137852231
pharmgkbrs137852231
gwascentralrs137852231
openSNPrs137852231
23andMers137852231
23andMe allrs137852231
SNP Nexus

SNPshotrs137852231
SNPdbers137852231
MSV3drs137852231
GWAS Ctlgrs137852231
Max Magnitude0
OMIM300746
Desc
Variant0020
Relatedalso
ClinVar
Risk rs137852231(C;C)
Alt rs137852231(C;C)
Reference rs137852231(A;A)
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.138623244A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011323.1,