rs121918486

Orientation

plus

Stabilized

plus

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

Make rs121918486(C;G)

Make rs121918486(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46739324

Gene

F2

is a	snp
is	mentioned by
dbSNP	rs121918486
dbSNP (classic)	rs121918486
ClinGen	rs121918486
ebi	rs121918486
HLI	rs121918486
Exac	rs121918486
Gnomad	rs121918486
Varsome	rs121918486
LitVar	rs121918486
Map	rs121918486
PheGenI	rs121918486
Biobank	rs121918486
1000 genomes	rs121918486
hgdp	rs121918486
ensembl	rs121918486
geneview	rs121918486
scholar	rs121918486
google	rs121918486
pharmgkb	rs121918486
gwascentral	rs121918486
openSNP	rs121918486
23andMe	rs121918486
SNPshot	rs121918486
SNPdbe	rs121918486
MSV3d	rs121918486
GWAS Ctlg	rs121918486

Max Magnitude

0

OMIM	176930
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121918486(G;G)
Alt	rs121918486(G;G)
Reference	Rs121918486(C;C)
Significance	Pathogenic
Disease	Hereditary factor II deficiency disease
Variation	info
Gene	F2
CLNDBN	Hereditary factor II deficiency disease
Reversed	0
HGVS	NC_000011.9:g.46760874C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014242.18,