rs104894418

Orientation

minus

Stabilized

minus

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

Make rs104894418(C;T)

Make rs104894418(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

108209531

Gene

LIG4

is a	snp
is	mentioned by
dbSNP	rs104894418
dbSNP (classic)	rs104894418
ClinGen	rs104894418
ebi	rs104894418
HLI	rs104894418
Exac	rs104894418
Gnomad	rs104894418
Varsome	rs104894418
LitVar	rs104894418
Map	rs104894418
PheGenI	rs104894418
Biobank	rs104894418
1000 genomes	rs104894418
hgdp	rs104894418
ensembl	rs104894418
geneview	rs104894418
scholar	rs104894418
google	rs104894418
pharmgkb	rs104894418
gwascentral	rs104894418
openSNP	rs104894418
23andMe	rs104894418
SNPshot	rs104894418
SNPdbe	rs104894418
MSV3d	rs104894418
GWAS Ctlg	rs104894418

Max Magnitude

0

OMIM	601837
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894418(G;G) rs104894418(T;T)
Alt	rs104894418(G;G) rs104894418(T;T)
Reference	Rs104894418(C;C)
Significance	Pathogenic
Disease	Lig4 syndrome
Variation	info
Gene	LIG4
CLNDBN	Lig4 syndrome
Reversed	1
HGVS	NC_000013.10:g.108861879G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008111.2,