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rs137852238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852238(A;A)
Make rs137852238(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551113
GeneF9
is asnp
is mentioned by
dbSNPrs137852238
ebirs137852238
HLIrs137852238
Exacrs137852238
Varsomers137852238
Maprs137852238
PheGenIrs137852238
hapmaprs137852238
1000 genomesrs137852238
hgdprs137852238
ensemblrs137852238
gopubmedrs137852238
geneviewrs137852238
scholarrs137852238
googlers137852238
pharmgkbrs137852238
gwascentralrs137852238
openSNPrs137852238
23andMers137852238
23andMe allrs137852238
SNP Nexus

SNPshotrs137852238
SNPdbers137852238
MSV3drs137852238
GWAS Ctlgrs137852238
Max Magnitude0
OMIM300746
Desc
Variant0027
Relatedalso
ClinVar
Risk rs137852238(A;A)
Alt rs137852238(A;A)
Reference rs137852238(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.138633272G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011331.7,