rs199469480

Orientation

plus

Stabilized

plus

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

Make rs199469480(A;T)

Make rs199469480(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127428540

Gene	LOC105373608, PROC

is a	snp
is	mentioned by
dbSNP	rs199469480
dbSNP (classic)	rs199469480
ClinGen	rs199469480
ebi	rs199469480
HLI	rs199469480
Exac	rs199469480
Gnomad	rs199469480
Varsome	rs199469480
LitVar	rs199469480
Map	rs199469480
PheGenI	rs199469480
Biobank	rs199469480
1000 genomes	rs199469480
hgdp	rs199469480
ensembl	rs199469480
geneview	rs199469480
scholar	rs199469480
google	rs199469480
pharmgkb	rs199469480
gwascentral	rs199469480
openSNP	rs199469480
23andMe	rs199469480
SNPshot	rs199469480
SNPdbe	rs199469480
MSV3d	rs199469480
GWAS Ctlg	rs199469480

Max Magnitude

0

ClinVar
Risk	rs199469480(T;T)
Alt	rs199469480(T;T)
Reference	Rs199469480(A;A)
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.128186116A>T
CLNSRC
CLNACC