rs869025198

Orientation

minus

Stabilized

minus

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

Make rs869025198(C;C)

Make rs869025198(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

215376610

Gene

FN1

is a	snp
is	mentioned by
dbSNP	rs869025198
dbSNP (classic)	rs869025198
ClinGen	rs869025198
ebi	rs869025198
HLI	rs869025198
Exac	rs869025198
Gnomad	rs869025198
Varsome	rs869025198
LitVar	rs869025198
Map	rs869025198
PheGenI	rs869025198
Biobank	rs869025198
1000 genomes	rs869025198
hgdp	rs869025198
ensembl	rs869025198
geneview	rs869025198
scholar	rs869025198
google	rs869025198
pharmgkb	rs869025198
gwascentral	rs869025198
openSNP	rs869025198
23andMe	rs869025198
SNPshot	rs869025198
SNPdbe	rs869025198
MSV3d	rs869025198
GWAS Ctlg	rs869025198

Max Magnitude

0

ClinVar
Risk	rs869025198(C;C)
Alt	rs869025198(C;C)
Reference	Rs869025198(G;G)
Significance	Pathogenic
Disease	Glomerulopathy with fibronectin deposits 2
Variation	info
Gene	FN1
CLNDBN	Glomerulopathy with fibronectin deposits 2
Reversed	1
HGVS	NC_000002.11:g.216241333C>G
CLNSRC
CLNACC	RCV000207361.1,