rs199469475

Orientation

plus

Stabilized

plus

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

Make rs199469475(-;G)

Make rs199469475(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127427142

Gene	LOC105373608, PROC

is a	snp
is	mentioned by
dbSNP	rs199469475
dbSNP (classic)	rs199469475
ClinGen	rs199469475
ebi	rs199469475
HLI	rs199469475
Exac	rs199469475
Gnomad	rs199469475
Varsome	rs199469475
LitVar	rs199469475
Map	rs199469475
PheGenI	rs199469475
Biobank	rs199469475
1000 genomes	rs199469475
hgdp	rs199469475
ensembl	rs199469475
geneview	rs199469475
scholar	rs199469475
google	rs199469475
pharmgkb	rs199469475
gwascentral	rs199469475
openSNP	rs199469475
23andMe	rs199469475
SNPshot	rs199469475
SNPdbe	rs199469475
MSV3d	rs199469475
GWAS Ctlg	rs199469475

Max Magnitude

0

ClinVar
Risk	rs199469475(G;G)
Alt	rs199469475(G;G)
Reference	Rs199469475(;)
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.128184718dupG
CLNSRC
CLNACC