rs796052476

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs796052476(-;G)

Make rs796052476(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767662

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs796052476
dbSNP (classic)	rs796052476
ClinGen	rs796052476
ebi	rs796052476
HLI	rs796052476
Exac	rs796052476
Gnomad	rs796052476
Varsome	rs796052476
LitVar	rs796052476
Map	rs796052476
PheGenI	rs796052476
Biobank	rs796052476
1000 genomes	rs796052476
hgdp	rs796052476
ensembl	rs796052476
geneview	rs796052476
scholar	rs796052476
google	rs796052476
pharmgkb	rs796052476
gwascentral	rs796052476
openSNP	rs796052476
23andMe	rs796052476
SNPshot	rs796052476
SNPdbe	rs796052476
MSV3d	rs796052476
GWAS Ctlg	rs796052476

Max Magnitude

0

ClinVar
Risk	rs796052476(G;G)
Alt	rs796052476(G;G)
Reference	Rs796052476(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29236868dupG
CLNSRC
CLNACC	RCV000187478.1,