rs368472521

Orientation

plus

Stabilized

plus

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

Make rs368472521(C;T)

Make rs368472521(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

58078747

Gene

FLNB

is a	snp
is	mentioned by
dbSNP	rs368472521
dbSNP (classic)	rs368472521
ClinGen	rs368472521
ebi	rs368472521
HLI	rs368472521
Exac	rs368472521
Gnomad	rs368472521
Varsome	rs368472521
LitVar	rs368472521
Map	rs368472521
PheGenI	rs368472521
Biobank	rs368472521
1000 genomes	rs368472521
hgdp	rs368472521
ensembl	rs368472521
geneview	rs368472521
scholar	rs368472521
google	rs368472521
pharmgkb	rs368472521
gwascentral	rs368472521
openSNP	rs368472521
23andMe	rs368472521
SNPshot	rs368472521
SNPdbe	rs368472521
MSV3d	rs368472521
GWAS Ctlg	rs368472521

Max Magnitude

0

ClinVar
Risk	rs368472521(T;T)
Alt	rs368472521(T;T)
Reference	Rs368472521(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FLNB
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.58064474C>T
CLNSRC
CLNACC	RCV000413979.1,