rs199469476

Orientation

plus

Stabilized

plus

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

Make rs199469476(A;A)

Make rs199469476(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127426181

Gene	LOC105373608, PROC

is a	snp
is	mentioned by
dbSNP	rs199469476
dbSNP (classic)	rs199469476
ClinGen	rs199469476
ebi	rs199469476
HLI	rs199469476
Exac	rs199469476
Gnomad	rs199469476
Varsome	rs199469476
LitVar	rs199469476
Map	rs199469476
PheGenI	rs199469476
Biobank	rs199469476
1000 genomes	rs199469476
hgdp	rs199469476
ensembl	rs199469476
geneview	rs199469476
scholar	rs199469476
google	rs199469476
pharmgkb	rs199469476
gwascentral	rs199469476
openSNP	rs199469476
23andMe	rs199469476
SNPshot	rs199469476
SNPdbe	rs199469476
MSV3d	rs199469476
GWAS Ctlg	rs199469476

Merged from

Rs28933987

Max Magnitude

0

ClinVar
Risk	rs199469476(A;A)
Alt	rs199469476(A;A)
Reference	Rs199469476(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.128183757G>A
CLNSRC
CLNACC