rs746167150

Orientation

plus

Stabilized

plus

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

Make rs746167150(C;T)

Make rs746167150(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

48437054

Gene

FBN1

is a	snp
is	mentioned by
dbSNP	rs746167150
dbSNP (classic)	rs746167150
ClinGen	rs746167150
ebi	rs746167150
HLI	rs746167150
Exac	rs746167150
Gnomad	rs746167150
Varsome	rs746167150
LitVar	rs746167150
Map	rs746167150
PheGenI	rs746167150
Biobank	rs746167150
1000 genomes	rs746167150
hgdp	rs746167150
ensembl	rs746167150
geneview	rs746167150
scholar	rs746167150
google	rs746167150
pharmgkb	rs746167150
gwascentral	rs746167150
openSNP	rs746167150
23andMe	rs746167150
SNPshot	rs746167150
SNPdbe	rs746167150
MSV3d	rs746167150
GWAS Ctlg	rs746167150

Max Magnitude

0

ClinVar
Risk	rs746167150(T;T)
Alt	rs746167150(T;T)
Reference	Rs746167150(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FBN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.48729251C>T
CLNSRC
CLNACC	RCV000181564.2,