rs199469479

Orientation

plus

Stabilized

plus

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

Make rs199469479(G;G)

Make rs199469479(G;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

127423087

Gene	MIR4783, PROC

is a	snp
is	mentioned by
dbSNP	rs199469479
dbSNP (classic)	rs199469479
ClinGen	rs199469479
ebi	rs199469479
HLI	rs199469479
Exac	rs199469479
Gnomad	rs199469479
Varsome	rs199469479
LitVar	rs199469479
Map	rs199469479
PheGenI	rs199469479
Biobank	rs199469479
1000 genomes	rs199469479
hgdp	rs199469479
ensembl	rs199469479
geneview	rs199469479
scholar	rs199469479
google	rs199469479
pharmgkb	rs199469479
gwascentral	rs199469479
openSNP	rs199469479
23andMe	rs199469479
SNPshot	rs199469479
SNPdbe	rs199469479
MSV3d	rs199469479
GWAS Ctlg	rs199469479

Max Magnitude

0

ClinVar
Risk	rs199469479(G;G)
Alt	rs199469479(G;G)
Reference	Rs199469479(T;T)
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.128180663T>G
CLNSRC
CLNACC