rs869025413

Orientation

minus

Stabilized

minus

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

Make rs869025413(C;C)

Make rs869025413(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

48430677

Gene

FBN1

is a	snp
is	mentioned by
dbSNP	rs869025413
dbSNP (classic)	rs869025413
ClinGen	rs869025413
ebi	rs869025413
HLI	rs869025413
Exac	rs869025413
Gnomad	rs869025413
Varsome	rs869025413
LitVar	rs869025413
Map	rs869025413
PheGenI	rs869025413
Biobank	rs869025413
1000 genomes	rs869025413
hgdp	rs869025413
ensembl	rs869025413
geneview	rs869025413
scholar	rs869025413
google	rs869025413
pharmgkb	rs869025413
gwascentral	rs869025413
openSNP	rs869025413
23andMe	rs869025413
SNPshot	rs869025413
SNPdbe	rs869025413
MSV3d	rs869025413
GWAS Ctlg	rs869025413

Max Magnitude

0

ClinVar
Risk	rs869025413(C;C)
Alt	rs869025413(C;C)
Reference	Rs869025413(T;T)
Significance	Probable-Pathogenic
Disease	Marfan syndrome
Variation	info
Gene	FBN1
CLNDBN	Marfan syndrome
Reversed	1
HGVS	NC_000015.9:g.48722874A>G
CLNSRC
CLNACC	RCV000208020.1,