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rs387906522

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906522(-;-)
Make rs387906522(-;T)
Make rs387906522(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position46723421
GeneF2
is asnp
is mentioned by
dbSNPrs387906522
ebirs387906522
HLIrs387906522
Exacrs387906522
Varsomers387906522
Maprs387906522
PheGenIrs387906522
hapmaprs387906522
1000 genomesrs387906522
hgdprs387906522
ensemblrs387906522
gopubmedrs387906522
geneviewrs387906522
scholarrs387906522
googlers387906522
pharmgkbrs387906522
gwascentralrs387906522
openSNPrs387906522
23andMers387906522
23andMe allrs387906522
SNP Nexus

SNPshotrs387906522
SNPdbers387906522
MSV3drs387906522
GWAS Ctlgrs387906522
Max Magnitude0
ClinVar
Risk rs387906522(T;T)
Alt rs387906522(T;T)
Reference rs387906522(;)
Significance Pathogenic
Disease Prothrombin deficiency
Variation info
Gene F2
CLNDBN Prothrombin deficiency, congenital
Reversed 0
HGVS NC_000011.9:g.46744971_46744972insT
CLNSRC OMIM Allelic Variant
CLNACC RCV000014236.16,