rs4775765

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(T;T)	0	common in complete genomics

Make rs4775765(C;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

48515440

Gene

FBN1

is a	snp
is	mentioned by
dbSNP	rs4775765
dbSNP (classic)	rs4775765
ClinGen	rs4775765
ebi	rs4775765
HLI	rs4775765
Exac	rs4775765
Gnomad	rs4775765
Varsome	rs4775765
LitVar	rs4775765
Map	rs4775765
PheGenI	rs4775765
Biobank	rs4775765
1000 genomes	rs4775765
hgdp	rs4775765
ensembl	rs4775765
geneview	rs4775765
scholar	rs4775765
google	rs4775765
pharmgkb	rs4775765
gwascentral	rs4775765
openSNP	rs4775765
23andMe	rs4775765
SNPshot	rs4775765
SNPdbe	rs4775765
MSV3d	rs4775765
GWAS Ctlg	rs4775765

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	Rs4775765(T;T)
Alt	Rs4775765(T;T)
Reference	Rs4775765(C;C)
Significance	Untested
Disease	not specified
Variation	info
Gene	FBN1
CLNDBN	not specified
Reversed	0
HGVS	NC_000015.9:g.48807637C>T
CLNSRC
CLNACC	RCV000223162.1,