rs781135153

Orientation

plus

Stabilized

plus

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

Make rs781135153(C;C)

Make rs781135153(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

128845989

Gene

FLNC

is a	snp
is	mentioned by
dbSNP	rs781135153
dbSNP (classic)	rs781135153
ClinGen	rs781135153
ebi	rs781135153
HLI	rs781135153
Exac	rs781135153
Gnomad	rs781135153
Varsome	rs781135153
LitVar	rs781135153
Map	rs781135153
PheGenI	rs781135153
Biobank	rs781135153
1000 genomes	rs781135153
hgdp	rs781135153
ensembl	rs781135153
geneview	rs781135153
scholar	rs781135153
google	rs781135153
pharmgkb	rs781135153
gwascentral	rs781135153
openSNP	rs781135153
23andMe	rs781135153
SNPshot	rs781135153
SNPdbe	rs781135153
MSV3d	rs781135153
GWAS Ctlg	rs781135153

Max Magnitude

0

ClinVar
Risk	rs781135153(C;C)
Alt	rs781135153(C;C)
Reference	Rs781135153(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FLNC
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.128486043G>C
CLNSRC
CLNACC	RCV000483809.1,