rs863223563

Orientation

minus

Stabilized

minus

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

Make rs863223563(A;A)

Make rs863223563(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

128344447

Gene

FBN2

is a	snp
is	mentioned by
dbSNP	rs863223563
dbSNP (classic)	rs863223563
ClinGen	rs863223563
ebi	rs863223563
HLI	rs863223563
Exac	rs863223563
Gnomad	rs863223563
Varsome	rs863223563
LitVar	rs863223563
Map	rs863223563
PheGenI	rs863223563
Biobank	rs863223563
1000 genomes	rs863223563
hgdp	rs863223563
ensembl	rs863223563
geneview	rs863223563
scholar	rs863223563
google	rs863223563
pharmgkb	rs863223563
gwascentral	rs863223563
openSNP	rs863223563
23andMe	rs863223563
SNPshot	rs863223563
SNPdbe	rs863223563
MSV3d	rs863223563
GWAS Ctlg	rs863223563

Max Magnitude

0

ClinVar
Risk	rs863223563(A;A)
Alt	rs863223563(A;A)
Reference	Rs863223563(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FBN2
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.127680139C>T
CLNSRC
CLNACC	RCV000196420.1,