rs199502880

Orientation

minus

Stabilized

minus

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

Make rs199502880(A;G)

Make rs199502880(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767965

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs199502880
dbSNP (classic)	rs199502880
ClinGen	rs199502880
ebi	rs199502880
HLI	rs199502880
Exac	rs199502880
Gnomad	rs199502880
Varsome	rs199502880
LitVar	rs199502880
Map	rs199502880
PheGenI	rs199502880
Biobank	rs199502880
1000 genomes	rs199502880
hgdp	rs199502880
ensembl	rs199502880
geneview	rs199502880
scholar	rs199502880
google	rs199502880
pharmgkb	rs199502880
gwascentral	rs199502880
openSNP	rs199502880
23andMe	rs199502880
SNPshot	rs199502880
SNPdbe	rs199502880
MSV3d	rs199502880
GWAS Ctlg	rs199502880

Max Magnitude

0

ClinVar
Risk	rs199502880(G;G)
Alt	rs199502880(G;G)
Reference	Rs199502880(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.29237171T>A
CLNSRC
CLNACC	RCV000187461.1,