rs199469470

Orientation

plus

Stabilized

plus

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

Make rs199469470(G;G)

Make rs199469470(G;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127426090

Gene	LOC105373608, PROC

is a	snp
is	mentioned by
dbSNP	rs199469470
dbSNP (classic)	rs199469470
ClinGen	rs199469470
ebi	rs199469470
HLI	rs199469470
Exac	rs199469470
Gnomad	rs199469470
Varsome	rs199469470
LitVar	rs199469470
Map	rs199469470
PheGenI	rs199469470
Biobank	rs199469470
1000 genomes	rs199469470
hgdp	rs199469470
ensembl	rs199469470
geneview	rs199469470
scholar	rs199469470
google	rs199469470
pharmgkb	rs199469470
gwascentral	rs199469470
openSNP	rs199469470
23andMe	rs199469470
SNPshot	rs199469470
SNPdbe	rs199469470
MSV3d	rs199469470
GWAS Ctlg	rs199469470

Max Magnitude

0

ClinVar
Risk	rs199469470(G;G)
Alt	rs199469470(G;G)
Reference	Rs199469470(T;T)
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.128183666T>G
CLNSRC
CLNACC