rs387907201

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs387907201(G;T)

Make rs387907201(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46739326

Gene

F2

is a	snp
is	mentioned by
dbSNP	rs387907201
dbSNP (classic)	rs387907201
ClinGen	rs387907201
ebi	rs387907201
HLI	rs387907201
Exac	rs387907201
Gnomad	rs387907201
Varsome	rs387907201
LitVar	rs387907201
Map	rs387907201
PheGenI	rs387907201
Biobank	rs387907201
1000 genomes	rs387907201
hgdp	rs387907201
ensembl	rs387907201
geneview	rs387907201
scholar	rs387907201
google	rs387907201
pharmgkb	rs387907201
gwascentral	rs387907201
openSNP	rs387907201
23andMe	rs387907201
SNPshot	rs387907201
SNPdbe	rs387907201
MSV3d	rs387907201
GWAS Ctlg	rs387907201

Max Magnitude

0

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	RCV000024607.28,