rs6828

plus

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

Make rs6828(C;C)

Make rs6828(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

1776708

Gene

SERPINF1

is a	snp
is	mentioned by
dbSNP	rs6828
dbSNP (classic)	rs6828
ClinGen	rs6828
ebi	rs6828
HLI	rs6828
Exac	rs6828
Gnomad	rs6828
Varsome	rs6828
LitVar	rs6828
Map	rs6828
PheGenI	rs6828
Biobank	rs6828
1000 genomes	rs6828
hgdp	rs6828
ensembl	rs6828
geneview	rs6828
scholar	rs6828
google	rs6828
pharmgkb	rs6828
gwascentral	rs6828
openSNP	rs6828
23andMe	rs6828
SNPshot	rs6828
SNPdbe	rs6828
MSV3d	rs6828
GWAS Ctlg	rs6828

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 28420811] The T Allele of rs8075977 in the 5'-Flanking Region of the PEDF Gene Is Associated with Reduced Risk of Coronary Artery Disease in Elderly Chinese Men.

ClinVar
Risk	rs6828(C;C) rs6828(G;G)
Alt	rs6828(C;C) rs6828(G;G)
Reference	Rs6828(T;T)
Significance	Non-pathogenic
Disease	Osteogenesis Imperfecta
Variation	info
Gene	SERPINF1
CLNDBN	Osteogenesis Imperfecta, Recessive
Reversed	0
HGVS	NC_000017.10:g.1680002T>C
CLNSRC
CLNACC	RCV000333112.1,