rs121918484

Orientation

plus

Stabilized

plus

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

Make rs121918484(A;A)

Make rs121918484(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46726761

Gene

F2

is a	snp
is	mentioned by
dbSNP	rs121918484
dbSNP (classic)	rs121918484
ClinGen	rs121918484
ebi	rs121918484
HLI	rs121918484
Exac	rs121918484
Gnomad	rs121918484
Varsome	rs121918484
LitVar	rs121918484
Map	rs121918484
PheGenI	rs121918484
Biobank	rs121918484
1000 genomes	rs121918484
hgdp	rs121918484
ensembl	rs121918484
geneview	rs121918484
scholar	rs121918484
google	rs121918484
pharmgkb	rs121918484
gwascentral	rs121918484
openSNP	rs121918484
23andMe	rs121918484
SNPshot	rs121918484
SNPdbe	rs121918484
MSV3d	rs121918484
GWAS Ctlg	rs121918484

Max Magnitude

0

OMIM	176930
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121918484(A;A)
Alt	rs121918484(A;A)
Reference	Rs121918484(G;G)
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.46748311G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014240.25,