rs199469481

Orientation

plus

Stabilized

plus

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

Make rs199469481(A;G)

Make rs199469481(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127421420

Gene

PROC

is a	snp
is	mentioned by
dbSNP	rs199469481
dbSNP (classic)	rs199469481
ClinGen	rs199469481
ebi	rs199469481
HLI	rs199469481
Exac	rs199469481
Gnomad	rs199469481
Varsome	rs199469481
LitVar	rs199469481
Map	rs199469481
PheGenI	rs199469481
Biobank	rs199469481
1000 genomes	rs199469481
hgdp	rs199469481
ensembl	rs199469481
geneview	rs199469481
scholar	rs199469481
google	rs199469481
pharmgkb	rs199469481
gwascentral	rs199469481
openSNP	rs199469481
23andMe	rs199469481
SNPshot	rs199469481
SNPdbe	rs199469481
MSV3d	rs199469481
GWAS Ctlg	rs199469481

Max Magnitude

0

ClinVar
Risk	rs199469481(G;G)
Alt	rs199469481(G;G)
Reference	Rs199469481(A;A)
Significance	Probable-Pathogenic
Disease	Thrombophilia
Variation	info
Gene	PROC
CLNDBN	Thrombophilia, hereditary, due to protein c deficiency, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.128178996A>G
CLNSRC
CLNACC