rs886037777

Orientation

minus

Stabilized

minus

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

Make rs886037777(C;C)

Make rs886037777(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

108209957

Gene

LIG4

is a	snp
is	mentioned by
dbSNP	rs886037777
dbSNP (classic)	rs886037777
ClinGen	rs886037777
ebi	rs886037777
HLI	rs886037777
Exac	rs886037777
Gnomad	rs886037777
Varsome	rs886037777
LitVar	rs886037777
Map	rs886037777
PheGenI	rs886037777
Biobank	rs886037777
1000 genomes	rs886037777
hgdp	rs886037777
ensembl	rs886037777
geneview	rs886037777
scholar	rs886037777
google	rs886037777
pharmgkb	rs886037777
gwascentral	rs886037777
openSNP	rs886037777
23andMe	rs886037777
SNPshot	rs886037777
SNPdbe	rs886037777
MSV3d	rs886037777
GWAS Ctlg	rs886037777

Max Magnitude

0

ClinVar
Risk	rs886037777(C;C)
Alt	rs886037777(C;C)
Reference	Rs886037777(T;T)
Significance	Probable-Pathogenic
Disease	Lig4 syndrome
Variation	info
Gene	LIG4
CLNDBN	Lig4 syndrome
Reversed	1
HGVS	NC_000013.10:g.108862305A>G
CLNSRC
CLNACC	RCV000241548.1,