rs770606675

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.5	Myofibrillar Myopathy

Make rs770606675(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

128841304

Gene

FLNC

is a	snp
is	mentioned by
dbSNP	rs770606675
dbSNP (classic)	rs770606675
ClinGen	rs770606675
ebi	rs770606675
HLI	rs770606675
Exac	rs770606675
Gnomad	rs770606675
Varsome	rs770606675
LitVar	rs770606675
Map	rs770606675
PheGenI	rs770606675
Biobank	rs770606675
1000 genomes	rs770606675
hgdp	rs770606675
ensembl	rs770606675
geneview	rs770606675
scholar	rs770606675
google	rs770606675
pharmgkb	rs770606675
gwascentral	rs770606675
openSNP	rs770606675
23andMe	rs770606675
SNPshot	rs770606675
SNPdbe	rs770606675
MSV3d	rs770606675
GWAS Ctlg	rs770606675

Max Magnitude

6.5

ClinVar
Risk	rs770606675(G;G) rs770606675(T;T)
Alt	rs770606675(G;G) rs770606675(T;T)
Reference	Rs770606675(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FLNC
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.128481358C>T
CLNSRC
CLNACC	RCV000479811.1,