rs863223628

Orientation

minus

Stabilized

minus

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

Make rs863223628(A;C)

Make rs863223628(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

154367955

Gene

FLNA

is a	snp
is	mentioned by
dbSNP	rs863223628
dbSNP (classic)	rs863223628
ClinGen	rs863223628
ebi	rs863223628
HLI	rs863223628
Exac	rs863223628
Gnomad	rs863223628
Varsome	rs863223628
LitVar	rs863223628
Map	rs863223628
PheGenI	rs863223628
Biobank	rs863223628
1000 genomes	rs863223628
hgdp	rs863223628
ensembl	rs863223628
geneview	rs863223628
scholar	rs863223628
google	rs863223628
pharmgkb	rs863223628
gwascentral	rs863223628
openSNP	rs863223628
23andMe	rs863223628
SNPshot	rs863223628
SNPdbe	rs863223628
MSV3d	rs863223628
GWAS Ctlg	rs863223628

Max Magnitude

0

ClinVar
Risk	rs863223628(C;C)
Alt	rs863223628(C;C)
Reference	Rs863223628(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLNA
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153596323T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000199318.1,