rs863223632

Orientation

minus

Stabilized

minus

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

Make rs863223632(-;-)

Make rs863223632(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

154359790

Gene

FLNA

is a	snp
is	mentioned by
dbSNP	rs863223632
dbSNP (classic)	rs863223632
ClinGen	rs863223632
ebi	rs863223632
HLI	rs863223632
Exac	rs863223632
Gnomad	rs863223632
Varsome	rs863223632
LitVar	rs863223632
Map	rs863223632
PheGenI	rs863223632
Biobank	rs863223632
1000 genomes	rs863223632
hgdp	rs863223632
ensembl	rs863223632
geneview	rs863223632
scholar	rs863223632
google	rs863223632
pharmgkb	rs863223632
gwascentral	rs863223632
openSNP	rs863223632
23andMe	rs863223632
SNPshot	rs863223632
SNPdbe	rs863223632
MSV3d	rs863223632
GWAS Ctlg	rs863223632

Max Magnitude

0

ClinVar
Risk	rs863223632(-;-)
Alt	rs863223632(-;-)
Reference	Rs863223632(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FLNA
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.153588158delG
CLNSRC
CLNACC	RCV000199592.3,