rs1060499662

Orientation

minus

Stabilized

minus

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

Make rs1060499662(C;C)

Make rs1060499662(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

108208948

Gene

LIG4

is a	snp
is	mentioned by
dbSNP	rs1060499662
dbSNP (classic)	rs1060499662
ClinGen	rs1060499662
ebi	rs1060499662
HLI	rs1060499662
Exac	rs1060499662
Gnomad	rs1060499662
Varsome	rs1060499662
LitVar	rs1060499662
Map	rs1060499662
PheGenI	rs1060499662
Biobank	rs1060499662
1000 genomes	rs1060499662
hgdp	rs1060499662
ensembl	rs1060499662
geneview	rs1060499662
scholar	rs1060499662
google	rs1060499662
pharmgkb	rs1060499662
gwascentral	rs1060499662
openSNP	rs1060499662
23andMe	rs1060499662
SNPshot	rs1060499662
SNPdbe	rs1060499662
MSV3d	rs1060499662
GWAS Ctlg	rs1060499662

Max Magnitude

0

ClinVar
Risk	rs1060499662(C;C)
Alt	rs1060499662(C;C)
Reference	Rs1060499662(T;T)
Significance	Probable-Pathogenic
Disease	Lig4 syndrome
Variation	info
Gene	LIG4
CLNDBN	Lig4 syndrome
Reversed	1
HGVS	NC_000013.10:g.108861296A>G
CLNSRC
CLNACC	RCV000449526.1,