rs794728227

Orientation

minus

Stabilized

minus

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

Make rs794728227(A;A)

Make rs794728227(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

48468099

Gene

FBN1

is a	snp
is	mentioned by
dbSNP	rs794728227
dbSNP (classic)	rs794728227
ClinGen	rs794728227
ebi	rs794728227
HLI	rs794728227
Exac	rs794728227
Gnomad	rs794728227
Varsome	rs794728227
LitVar	rs794728227
Map	rs794728227
PheGenI	rs794728227
Biobank	rs794728227
1000 genomes	rs794728227
hgdp	rs794728227
ensembl	rs794728227
geneview	rs794728227
scholar	rs794728227
google	rs794728227
pharmgkb	rs794728227
gwascentral	rs794728227
openSNP	rs794728227
23andMe	rs794728227
SNPshot	rs794728227
SNPdbe	rs794728227
MSV3d	rs794728227
GWAS Ctlg	rs794728227

Max Magnitude

0

ClinVar
Risk	rs794728227(A;A)
Alt	rs794728227(A;A)
Reference	Rs794728227(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	FBN1
CLNDBN	not specified
Reversed	1
HGVS	NC_000015.9:g.48760296G>T
CLNSRC
CLNACC	RCV000181527.2,