rs886037830

Orientation

plus

Stabilized

plus

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

Make rs886037830(C;T)

Make rs886037830(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

128844045

Gene

FLNC

is a	snp
is	mentioned by
dbSNP	rs886037830
dbSNP (classic)	rs886037830
ClinGen	rs886037830
ebi	rs886037830
HLI	rs886037830
Exac	rs886037830
Gnomad	rs886037830
Varsome	rs886037830
LitVar	rs886037830
Map	rs886037830
PheGenI	rs886037830
Biobank	rs886037830
1000 genomes	rs886037830
hgdp	rs886037830
ensembl	rs886037830
geneview	rs886037830
scholar	rs886037830
google	rs886037830
pharmgkb	rs886037830
gwascentral	rs886037830
openSNP	rs886037830
23andMe	rs886037830
SNPshot	rs886037830
SNPdbe	rs886037830
MSV3d	rs886037830
GWAS Ctlg	rs886037830

Max Magnitude

0

ClinVar
Risk	rs886037830(T;T)
Alt	rs886037830(T;T)
Reference	Rs886037830(C;C)
Significance	Pathogenic
Disease	Primary dilated cardiomyopathy
Variation	info
Gene	FLNC
CLNDBN	Primary dilated cardiomyopathy
Reversed	0
HGVS	NC_000007.13:g.128484099C>T
CLNSRC
CLNACC	RCV000256190.1,