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rs137852264

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852264(G;T)
Make rs137852264(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561911
GeneF9
is asnp
is mentioned by
dbSNPrs137852264
ebirs137852264
HLIrs137852264
Exacrs137852264
Varsomers137852264
Maprs137852264
PheGenIrs137852264
hapmaprs137852264
1000 genomesrs137852264
hgdprs137852264
ensemblrs137852264
gopubmedrs137852264
geneviewrs137852264
scholarrs137852264
googlers137852264
pharmgkbrs137852264
gwascentralrs137852264
openSNPrs137852264
23andMers137852264
23andMe allrs137852264
SNP Nexus

SNPshotrs137852264
SNPdbers137852264
MSV3drs137852264
GWAS Ctlgrs137852264
Max Magnitude0
OMIM300746
Desc
Variant0062
Relatedalso
ClinVar
Risk rs137852264(T;T)
Alt rs137852264(T;T)
Reference rs137852264(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.138644070G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011364.3,