rs863223565

Orientation

minus

Stabilized

minus

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

Make rs863223565(A;A)

Make rs863223565(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

128338949

Gene

FBN2

is a	snp
is	mentioned by
dbSNP	rs863223565
dbSNP (classic)	rs863223565
ClinGen	rs863223565
ebi	rs863223565
HLI	rs863223565
Exac	rs863223565
Gnomad	rs863223565
Varsome	rs863223565
LitVar	rs863223565
Map	rs863223565
PheGenI	rs863223565
Biobank	rs863223565
1000 genomes	rs863223565
hgdp	rs863223565
ensembl	rs863223565
geneview	rs863223565
scholar	rs863223565
google	rs863223565
pharmgkb	rs863223565
gwascentral	rs863223565
openSNP	rs863223565
23andMe	rs863223565
SNPshot	rs863223565
SNPdbe	rs863223565
MSV3d	rs863223565
GWAS Ctlg	rs863223565

Max Magnitude

0

ClinVar
Risk	rs863223565(A;A)
Alt	rs863223565(A;A)
Reference	Rs863223565(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FBN2
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.127674641C>T
CLNSRC
CLNACC	RCV000200568.1,