rs794728267

Orientation

minus

Stabilized

minus

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

Make rs794728267(C;C)

Make rs794728267(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

48427639

Gene

FBN1

is a	snp
is	mentioned by
dbSNP	rs794728267
dbSNP (classic)	rs794728267
ClinGen	rs794728267
ebi	rs794728267
HLI	rs794728267
Exac	rs794728267
Gnomad	rs794728267
Varsome	rs794728267
LitVar	rs794728267
Map	rs794728267
PheGenI	rs794728267
Biobank	rs794728267
1000 genomes	rs794728267
hgdp	rs794728267
ensembl	rs794728267
geneview	rs794728267
scholar	rs794728267
google	rs794728267
pharmgkb	rs794728267
gwascentral	rs794728267
openSNP	rs794728267
23andMe	rs794728267
SNPshot	rs794728267
SNPdbe	rs794728267
MSV3d	rs794728267
GWAS Ctlg	rs794728267

Max Magnitude

0

ClinVar
Risk	rs794728267(C;C)
Alt	rs794728267(C;C)
Reference	Rs794728267(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FBN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.48719836A>G
CLNSRC
CLNACC	RCV000181594.1,