rs786205178

Orientation

minus

Stabilized

minus

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

Make rs786205178(-;-)

Make rs786205178(-;TCAG)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154352312

Gene

FLNA

is a	snp
is	mentioned by
dbSNP	rs786205178
dbSNP (classic)	rs786205178
ClinGen	rs786205178
ebi	rs786205178
HLI	rs786205178
Exac	rs786205178
Gnomad	rs786205178
Varsome	rs786205178
LitVar	rs786205178
Map	rs786205178
PheGenI	rs786205178
Biobank	rs786205178
1000 genomes	rs786205178
hgdp	rs786205178
ensembl	rs786205178
geneview	rs786205178
scholar	rs786205178
google	rs786205178
pharmgkb	rs786205178
gwascentral	rs786205178
openSNP	rs786205178
23andMe	rs786205178
SNPshot	rs786205178
SNPdbe	rs786205178
MSV3d	rs786205178
GWAS Ctlg	rs786205178

Max Magnitude

0

ClinVar
Risk	rs786205178(-;-)
Alt	rs786205178(-;-)
Reference	Rs786205178(TCAG;TCAG)
Significance	Pathogenic
Disease	Periventricular nodular heterotopia 1 not provided
Variation	info
Gene	FLNA
CLNDBN	Periventricular nodular heterotopia 1 not provided
Reversed	1
HGVS	NC_000023.10:g.153580680_153580683delCTGA
CLNSRC
CLNACC	RCV000170398.1, RCV000199583.1,