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rs387907201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907201(G;T)
Make rs387907201(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position46739326
GeneF2
is asnp
is mentioned by
dbSNPrs387907201
ebirs387907201
HLIrs387907201
Exacrs387907201
Varsomers387907201
Maprs387907201
PheGenIrs387907201
hapmaprs387907201
1000 genomesrs387907201
hgdprs387907201
ensemblrs387907201
gopubmedrs387907201
geneviewrs387907201
scholarrs387907201
googlers387907201
pharmgkbrs387907201
gwascentralrs387907201
openSNPrs387907201
23andMers387907201
23andMe allrs387907201
SNP Nexus

SNPshotrs387907201
SNPdbers387907201
MSV3drs387907201
GWAS Ctlgrs387907201
Max Magnitude0
ClinVar
Risk rs387907201(T;T)
Alt rs387907201(T;T)
Reference rs387907201(G;G)
Significance Other
Disease Thrombophilia
Variation info
Gene F2
CLNDBN Thrombophilia
Reversed 0
HGVS NC_000011.9:g.46760876G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024607.27,