rs869312961

Orientation

plus

Stabilized

plus

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

Make rs869312961(C;G)

Make rs869312961(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

28768055

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs869312961
dbSNP (classic)	rs869312961
ClinGen	rs869312961
ebi	rs869312961
HLI	rs869312961
Exac	rs869312961
Gnomad	rs869312961
Varsome	rs869312961
LitVar	rs869312961
Map	rs869312961
PheGenI	rs869312961
Biobank	rs869312961
1000 genomes	rs869312961
hgdp	rs869312961
ensembl	rs869312961
geneview	rs869312961
scholar	rs869312961
google	rs869312961
pharmgkb	rs869312961
gwascentral	rs869312961
openSNP	rs869312961
23andMe	rs869312961
SNPshot	rs869312961
SNPdbe	rs869312961
MSV3d	rs869312961
GWAS Ctlg	rs869312961

Max Magnitude

0

ClinVar
Risk	rs869312961(G;G)
Alt	rs869312961(G;G)
Reference	Rs869312961(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	FOXG1
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000014.8:g.29237261C>G
CLNSRC
CLNACC	RCV000210671.1,