rs786205194

Orientation

minus

Stabilized

minus

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

Make rs786205194(-;-)

Make rs786205194(-;GC)

Reference

GRCh38.p2 38.2/146

Chromosome

X

Position

154358336

Gene

FLNA

is a	snp
is	mentioned by
dbSNP	rs786205194
dbSNP (classic)	rs786205194
ClinGen	rs786205194
ebi	rs786205194
HLI	rs786205194
Exac	rs786205194
Gnomad	rs786205194
Varsome	rs786205194
LitVar	rs786205194
Map	rs786205194
PheGenI	rs786205194
Biobank	rs786205194
1000 genomes	rs786205194
hgdp	rs786205194
ensembl	rs786205194
geneview	rs786205194
scholar	rs786205194
google	rs786205194
pharmgkb	rs786205194
gwascentral	rs786205194
openSNP	rs786205194
23andMe	rs786205194
SNPshot	rs786205194
SNPdbe	rs786205194
MSV3d	rs786205194
GWAS Ctlg	rs786205194

Max Magnitude

0

ClinVar
Risk	rs786205194(-;-)
Alt	rs786205194(-;-)
Reference	Rs786205194(GC;GC)
Significance	Probable-Pathogenic
Disease	Periventricular nodular heterotopia 1
Variation	info
Gene	FLNA
CLNDBN	Periventricular nodular heterotopia 1
Reversed	1
HGVS	NC_000023.10:g.153586704_153586705delGC
CLNSRC	Claritas Genomics
CLNACC	RCV000170416.1,