rs886037829

Orientation

plus

Stabilized

plus

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

Make rs886037829(C;G)

Make rs886037829(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

128830955

Gene

FLNC

is a	snp
is	mentioned by
dbSNP	rs886037829
dbSNP (classic)	rs886037829
ClinGen	rs886037829
ebi	rs886037829
HLI	rs886037829
Exac	rs886037829
Gnomad	rs886037829
Varsome	rs886037829
LitVar	rs886037829
Map	rs886037829
PheGenI	rs886037829
Biobank	rs886037829
1000 genomes	rs886037829
hgdp	rs886037829
ensembl	rs886037829
geneview	rs886037829
scholar	rs886037829
google	rs886037829
pharmgkb	rs886037829
gwascentral	rs886037829
openSNP	rs886037829
23andMe	rs886037829
SNPshot	rs886037829
SNPdbe	rs886037829
MSV3d	rs886037829
GWAS Ctlg	rs886037829

Max Magnitude

0

ClinVar
Risk	rs886037829(G;G)
Alt	rs886037829(G;G)
Reference	Rs886037829(C;C)
Significance	Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	FLNC
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000007.13:g.128471009C>G
CLNSRC
CLNACC	RCV000256190.1,