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rs137852276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852276(G;T)
Make rs137852276(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561917
GeneF9
is asnp
is mentioned by
dbSNPrs137852276
ebirs137852276
HLIrs137852276
Exacrs137852276
Varsomers137852276
Maprs137852276
PheGenIrs137852276
hapmaprs137852276
1000 genomesrs137852276
hgdprs137852276
ensemblrs137852276
gopubmedrs137852276
geneviewrs137852276
scholarrs137852276
googlers137852276
pharmgkbrs137852276
gwascentralrs137852276
openSNPrs137852276
23andMers137852276
23andMe allrs137852276
SNP Nexus

SNPshotrs137852276
SNPdbers137852276
MSV3drs137852276
GWAS Ctlgrs137852276
Max Magnitude0
OMIM300746
Desc
Variant0093
Relatedalso
ClinVar
Risk rs137852276(T;T)
Alt rs137852276(T;T)
Reference rs137852276(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.138644076G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011395.5,