rs786205183

Orientation

minus

Stabilized

minus

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

Make rs786205183(A;G)

Make rs786205183(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154364721

Gene

FLNA

is a	snp
is	mentioned by
dbSNP	rs786205183
dbSNP (classic)	rs786205183
ClinGen	rs786205183
ebi	rs786205183
HLI	rs786205183
Exac	rs786205183
Gnomad	rs786205183
Varsome	rs786205183
LitVar	rs786205183
Map	rs786205183
PheGenI	rs786205183
Biobank	rs786205183
1000 genomes	rs786205183
hgdp	rs786205183
ensembl	rs786205183
geneview	rs786205183
scholar	rs786205183
google	rs786205183
pharmgkb	rs786205183
gwascentral	rs786205183
openSNP	rs786205183
23andMe	rs786205183
SNPshot	rs786205183
SNPdbe	rs786205183
MSV3d	rs786205183
GWAS Ctlg	rs786205183

Max Magnitude

0

ClinVar
Risk	rs786205183(G;G)
Alt	rs786205183(G;G)
Reference	Rs786205183(A;A)
Significance	Pathogenic
Disease	Periventricular nodular heterotopia 1
Variation	info
Gene	FLNA
CLNDBN	Periventricular nodular heterotopia 1
Reversed	1
HGVS	NC_000023.10:g.153593089T>C
CLNSRC
CLNACC	RCV000170404.1,