rs397515756

Orientation

minus

Stabilized

minus

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

Make rs397515756(A;G)

Make rs397515756(G;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

48516364

Gene

FBN1

is a	snp
is	mentioned by
dbSNP	rs397515756
dbSNP (classic)	rs397515756
ClinGen	rs397515756
ebi	rs397515756
HLI	rs397515756
Exac	rs397515756
Gnomad	rs397515756
Varsome	rs397515756
LitVar	rs397515756
Map	rs397515756
PheGenI	rs397515756
Biobank	rs397515756
1000 genomes	rs397515756
hgdp	rs397515756
ensembl	rs397515756
geneview	rs397515756
scholar	rs397515756
google	rs397515756
pharmgkb	rs397515756
gwascentral	rs397515756
openSNP	rs397515756
23andMe	rs397515756
SNPshot	rs397515756
SNPdbe	rs397515756
MSV3d	rs397515756
GWAS Ctlg	rs397515756

Max Magnitude

0

ClinVar
Risk	rs397515756(C;C) rs397515756(G;G)
Alt	rs397515756(C;C) rs397515756(G;G)
Reference	Rs397515756(A;A)
Significance	Pathogenic
Disease	Marfan syndrome not provided
Variation	info
Gene	FBN1
CLNDBN	Marfan syndrome not provided
Reversed	1
HGVS	NC_000015.9:g.48808561T>C; NC_000015.9:g.48808561T>G
CLNSRC	ClinVar
CLNACC	RCV000035116.2, RCV000480005.1, RCV000181426.1,