rs199469469

Orientation

plus

Stabilized

plus

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

Make rs199469469(-;-)

Make rs199469469(-;AAG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127426123

Gene	LOC105373608, PROC

is a	snp
is	mentioned by
dbSNP	rs199469469
dbSNP (classic)	rs199469469
ClinGen	rs199469469
ebi	rs199469469
HLI	rs199469469
Exac	rs199469469
Gnomad	rs199469469
Varsome	rs199469469
LitVar	rs199469469
Map	rs199469469
PheGenI	rs199469469
Biobank	rs199469469
1000 genomes	rs199469469
hgdp	rs199469469
ensembl	rs199469469
geneview	rs199469469
scholar	rs199469469
google	rs199469469
pharmgkb	rs199469469
gwascentral	rs199469469
openSNP	rs199469469
23andMe	rs199469469
SNPshot	rs199469469
SNPdbe	rs199469469
MSV3d	rs199469469
GWAS Ctlg	rs199469469

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs199469469(AAG;AAG)
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.128183699_128183701delAAG
CLNSRC
CLNACC