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rs137852236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852236(A;T)
Make rs137852236(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139548467
GeneF9
is asnp
is mentioned by
dbSNPrs137852236
ebirs137852236
HLIrs137852236
Exacrs137852236
Varsomers137852236
Maprs137852236
PheGenIrs137852236
hapmaprs137852236
1000 genomesrs137852236
hgdprs137852236
ensemblrs137852236
gopubmedrs137852236
geneviewrs137852236
scholarrs137852236
googlers137852236
pharmgkbrs137852236
gwascentralrs137852236
openSNPrs137852236
23andMers137852236
23andMe allrs137852236
SNP Nexus

SNPshotrs137852236
SNPdbers137852236
MSV3drs137852236
GWAS Ctlgrs137852236
Max Magnitude0
OMIM300746
Desc
Variant0025
Relatedalso
ClinVar
Risk rs137852236(T;T)
Alt rs137852236(T;T)
Reference rs137852236(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.138630626A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011328.7,