rs1057518165

Orientation

plus

Stabilized

plus

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

Make rs1057518165(C;G)

Make rs1057518165(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

28767924

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs1057518165
dbSNP (classic)	rs1057518165
ClinGen	rs1057518165
ebi	rs1057518165
HLI	rs1057518165
Exac	rs1057518165
Gnomad	rs1057518165
Varsome	rs1057518165
LitVar	rs1057518165
Map	rs1057518165
PheGenI	rs1057518165
Biobank	rs1057518165
1000 genomes	rs1057518165
hgdp	rs1057518165
ensembl	rs1057518165
geneview	rs1057518165
scholar	rs1057518165
google	rs1057518165
pharmgkb	rs1057518165
gwascentral	rs1057518165
openSNP	rs1057518165
23andMe	rs1057518165
SNPshot	rs1057518165
SNPdbe	rs1057518165
MSV3d	rs1057518165
GWAS Ctlg	rs1057518165

Max Magnitude

0

ClinVar
Risk	rs1057518165(G;G)
Alt	rs1057518165(G;G)
Reference	Rs1057518165(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29237130C>G
CLNSRC
CLNACC	RCV000414314.1,