rs1057518196

Orientation

plus

Stabilized

plus

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

Make rs1057518196(CG;GTC)

Make rs1057518196(GTC;GTC)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

28768439

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs1057518196
dbSNP (classic)	rs1057518196
ClinGen	rs1057518196
ebi	rs1057518196
HLI	rs1057518196
Exac	rs1057518196
Gnomad	rs1057518196
Varsome	rs1057518196
LitVar	rs1057518196
Map	rs1057518196
PheGenI	rs1057518196
Biobank	rs1057518196
1000 genomes	rs1057518196
hgdp	rs1057518196
ensembl	rs1057518196
geneview	rs1057518196
scholar	rs1057518196
google	rs1057518196
pharmgkb	rs1057518196
gwascentral	rs1057518196
openSNP	rs1057518196
23andMe	rs1057518196
SNPshot	rs1057518196
SNPdbe	rs1057518196
MSV3d	rs1057518196
GWAS Ctlg	rs1057518196

Max Magnitude

0

ClinVar
Risk	rs1057518196(GTC;GTC)
Alt	rs1057518196(GTC;GTC)
Reference	Rs1057518196(CG;CG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29237645_29237646delCGinsGTC
CLNSRC
CLNACC	RCV000414221.1,