rs199469474

Orientation

plus

Stabilized

plus

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

Make rs199469474(A;A)

Make rs199469474(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127423397

Gene	MIR4783, PROC

is a	snp
is	mentioned by
dbSNP	rs199469474
dbSNP (classic)	rs199469474
ClinGen	rs199469474
ebi	rs199469474
HLI	rs199469474
Exac	rs199469474
Gnomad	rs199469474
Varsome	rs199469474
LitVar	rs199469474
Map	rs199469474
PheGenI	rs199469474
Biobank	rs199469474
1000 genomes	rs199469474
hgdp	rs199469474
ensembl	rs199469474
geneview	rs199469474
scholar	rs199469474
google	rs199469474
pharmgkb	rs199469474
gwascentral	rs199469474
openSNP	rs199469474
23andMe	rs199469474
SNPshot	rs199469474
SNPdbe	rs199469474
MSV3d	rs199469474
GWAS Ctlg	rs199469474

Max Magnitude

0

ClinVar
Risk	rs199469474(A;A)
Alt	rs199469474(A;A)
Reference	Rs199469474(G;G)
Significance	Probable-Pathogenic
Disease	Thrombophilia
Variation	info
Gene	PROC MIR4783
CLNDBN	Thrombophilia, hereditary, due to protein c deficiency, autosomal dominant
Reversed	0
HGVS	NC_000002.11:g.128180973G>A
CLNSRC
CLNACC