rs772226399

Orientation

plus

Stabilized

plus

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

Make rs772226399(-;-)

Make rs772226399(-;TCTTT)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

108209994

Gene

LIG4

is a	snp
is	mentioned by
dbSNP	rs772226399
dbSNP (classic)	rs772226399
ClinGen	rs772226399
ebi	rs772226399
HLI	rs772226399
Exac	rs772226399
Gnomad	rs772226399
Varsome	rs772226399
LitVar	rs772226399
Map	rs772226399
PheGenI	rs772226399
Biobank	rs772226399
1000 genomes	rs772226399
hgdp	rs772226399
ensembl	rs772226399
geneview	rs772226399
scholar	rs772226399
google	rs772226399
pharmgkb	rs772226399
gwascentral	rs772226399
openSNP	rs772226399
23andMe	rs772226399
SNPshot	rs772226399
SNPdbe	rs772226399
MSV3d	rs772226399
GWAS Ctlg	rs772226399

Max Magnitude

0

ClinVar
Risk	rs772226399(-;-)
Alt	rs772226399(-;-)
Reference	Rs772226399(TCTTT;TCTTT)
Significance	Pathogenic
Disease	LIG4-Related Disorders not provided
Variation	info
Gene	LIG4
CLNDBN	LIG4-Related Disorders not provided
Reversed	0
HGVS	NC_000013.10:g.108862342_108862346delTCTTT
CLNSRC	Illumina
CLNACC	RCV000267680.1, RCV000338918.1,