rs863223568

Orientation

minus

Stabilized

minus

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

Make rs863223568(C;C)

Make rs863223568(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

128336056

Gene

FBN2

is a	snp
is	mentioned by
dbSNP	rs863223568
dbSNP (classic)	rs863223568
ClinGen	rs863223568
ebi	rs863223568
HLI	rs863223568
Exac	rs863223568
Gnomad	rs863223568
Varsome	rs863223568
LitVar	rs863223568
Map	rs863223568
PheGenI	rs863223568
Biobank	rs863223568
1000 genomes	rs863223568
hgdp	rs863223568
ensembl	rs863223568
geneview	rs863223568
scholar	rs863223568
google	rs863223568
pharmgkb	rs863223568
gwascentral	rs863223568
openSNP	rs863223568
23andMe	rs863223568
SNPshot	rs863223568
SNPdbe	rs863223568
MSV3d	rs863223568
GWAS Ctlg	rs863223568

Max Magnitude

0

ClinVar
Risk	rs863223568(C;C)
Alt	rs863223568(C;C)
Reference	Rs863223568(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FBN2
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.127671748A>G
CLNSRC
CLNACC	RCV000198913.1,