rs796052485

Orientation

plus

Stabilized

plus

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

Make rs796052485(ACCG;ACCG)

Make rs796052485(ACCG;GC)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

28767504

Gene

FOXG1

is a	snp
is	mentioned by
dbSNP	rs796052485
dbSNP (classic)	rs796052485
ClinGen	rs796052485
ebi	rs796052485
HLI	rs796052485
Exac	rs796052485
Gnomad	rs796052485
Varsome	rs796052485
LitVar	rs796052485
Map	rs796052485
PheGenI	rs796052485
Biobank	rs796052485
1000 genomes	rs796052485
hgdp	rs796052485
ensembl	rs796052485
geneview	rs796052485
scholar	rs796052485
google	rs796052485
pharmgkb	rs796052485
gwascentral	rs796052485
openSNP	rs796052485
23andMe	rs796052485
SNPshot	rs796052485
SNPdbe	rs796052485
MSV3d	rs796052485
GWAS Ctlg	rs796052485

Max Magnitude

0

ClinVar
Risk	rs796052485(ACCG;ACCG)
Alt	rs796052485(ACCG;ACCG)
Reference	Rs796052485(GC;GC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	FOXG1
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.29236710_29236711delGCinsACCG
CLNSRC
CLNACC	RCV000187487.1,