rs121918483

Orientation

plus

Stabilized

plus

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

Make rs121918483(A;A)

Make rs121918483(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46726734

Gene

F2

is a	snp
is	mentioned by
dbSNP	rs121918483
dbSNP (classic)	rs121918483
ClinGen	rs121918483
ebi	rs121918483
HLI	rs121918483
Exac	rs121918483
Gnomad	rs121918483
Varsome	rs121918483
LitVar	rs121918483
Map	rs121918483
PheGenI	rs121918483
Biobank	rs121918483
1000 genomes	rs121918483
hgdp	rs121918483
ensembl	rs121918483
geneview	rs121918483
scholar	rs121918483
google	rs121918483
pharmgkb	rs121918483
gwascentral	rs121918483
openSNP	rs121918483
23andMe	rs121918483
SNPshot	rs121918483
SNPdbe	rs121918483
MSV3d	rs121918483
GWAS Ctlg	rs121918483

Max Magnitude

0

OMIM	176930
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121918483(A;A)
Alt	rs121918483(A;A)
Reference	Rs121918483(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.46748284G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014239.24,