rs797046135

Orientation

plus

Stabilized

plus

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

Make rs797046135(C;T)

Make rs797046135(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

28524525

Gene

FOXN1

is a	snp
is	mentioned by
dbSNP	rs797046135
dbSNP (classic)	rs797046135
ClinGen	rs797046135
ebi	rs797046135
HLI	rs797046135
Exac	rs797046135
Gnomad	rs797046135
Varsome	rs797046135
LitVar	rs797046135
Map	rs797046135
PheGenI	rs797046135
Biobank	rs797046135
1000 genomes	rs797046135
hgdp	rs797046135
ensembl	rs797046135
geneview	rs797046135
scholar	rs797046135
google	rs797046135
pharmgkb	rs797046135
gwascentral	rs797046135
openSNP	rs797046135
23andMe	rs797046135
SNPshot	rs797046135
SNPdbe	rs797046135
MSV3d	rs797046135
GWAS Ctlg	rs797046135

Max Magnitude

0

ClinVar
Risk	rs797046135(T;T)
Alt	rs797046135(T;T)
Reference	Rs797046135(C;C)
Significance	Probable-Pathogenic
Disease	Autistic disorder of childhood onset
Variation	info
Gene	FOXN1
CLNDBN	Autistic disorder of childhood onset
Reversed	0
HGVS	NC_000017.10:g.26851543C>T
CLNSRC	Laboratorio de Genetica Humana\x3bUniversidad de los Andes
CLNACC	RCV000192344.1,