rs199469482

Orientation

plus

Stabilized

plus

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

Make rs199469482(A;A)

Make rs199469482(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127421454

Gene

PROC

is a	snp
is	mentioned by
dbSNP	rs199469482
dbSNP (classic)	rs199469482
ClinGen	rs199469482
ebi	rs199469482
HLI	rs199469482
Exac	rs199469482
Gnomad	rs199469482
Varsome	rs199469482
LitVar	rs199469482
Map	rs199469482
PheGenI	rs199469482
Biobank	rs199469482
1000 genomes	rs199469482
hgdp	rs199469482
ensembl	rs199469482
geneview	rs199469482
scholar	rs199469482
google	rs199469482
pharmgkb	rs199469482
gwascentral	rs199469482
openSNP	rs199469482
23andMe	rs199469482
SNPshot	rs199469482
SNPdbe	rs199469482
MSV3d	rs199469482
GWAS Ctlg	rs199469482

Max Magnitude

0

ClinVar
Risk	rs199469482(A;A)
Alt	rs199469482(A;A)
Reference	Rs199469482(G;G)
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.128179030G>A
CLNSRC
CLNACC