rs797045403

Orientation

minus

Stabilized

minus

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

Make rs797045403(G;T)

Make rs797045403(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

142513500

Gene

ATR

is a	snp
is	mentioned by
dbSNP	rs797045403
dbSNP (classic)	rs797045403
ClinGen	rs797045403
ebi	rs797045403
HLI	rs797045403
Exac	rs797045403
Gnomad	rs797045403
Varsome	rs797045403
LitVar	rs797045403
Map	rs797045403
PheGenI	rs797045403
Biobank	rs797045403
1000 genomes	rs797045403
hgdp	rs797045403
ensembl	rs797045403
geneview	rs797045403
scholar	rs797045403
google	rs797045403
pharmgkb	rs797045403
gwascentral	rs797045403
openSNP	rs797045403
23andMe	rs797045403
SNPshot	rs797045403
SNPdbe	rs797045403
MSV3d	rs797045403
GWAS Ctlg	rs797045403

Max Magnitude

0

ClinVar
Risk	rs797045403(T;T)
Alt	rs797045403(T;T)
Reference	Rs797045403(G;G)
Significance	Pathogenic
Disease	Seckel syndrome 1
Variation	info
Gene	ATR
CLNDBN	Seckel syndrome 1
Reversed	1
HGVS	NC_000003.11:g.142232342C>A
CLNSRC
CLNACC	RCV000193414.1,