rs121918485

Orientation

plus

Stabilized

plus

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

Make rs121918485(A;A)

Make rs121918485(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46728139

Gene

F2

is a	snp
is	mentioned by
dbSNP	rs121918485
dbSNP (classic)	rs121918485
ClinGen	rs121918485
ebi	rs121918485
HLI	rs121918485
Exac	rs121918485
Gnomad	rs121918485
Varsome	rs121918485
LitVar	rs121918485
Map	rs121918485
PheGenI	rs121918485
Biobank	rs121918485
1000 genomes	rs121918485
hgdp	rs121918485
ensembl	rs121918485
geneview	rs121918485
scholar	rs121918485
google	rs121918485
pharmgkb	rs121918485
gwascentral	rs121918485
openSNP	rs121918485
23andMe	rs121918485
SNPshot	rs121918485
SNPdbe	rs121918485
MSV3d	rs121918485
GWAS Ctlg	rs121918485

Max Magnitude

0

OMIM	176930
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121918485(A;A)
Alt	rs121918485(A;A)
Reference	Rs121918485(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.46749689G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014241.23,