Have questions? Visit https://www.reddit.com/r/SNPedia

rs375554612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs375554612(-;-)
Make rs375554612(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position108209365
GeneLIG4
is asnp
is mentioned by
dbSNPrs375554612
dbSNP (classic)rs375554612
ClinGenrs375554612
ebirs375554612
HLIrs375554612
Exacrs375554612
Gnomadrs375554612
Varsomers375554612
LitVarrs375554612
Maprs375554612
PheGenIrs375554612
Biobankrs375554612
1000 genomesrs375554612
hgdprs375554612
ensemblrs375554612
geneviewrs375554612
scholarrs375554612
googlers375554612
pharmgkbrs375554612
gwascentralrs375554612
openSNPrs375554612
23andMers375554612
23andMe allrs375554612
SNPshotrs375554612
SNPdbers375554612
MSV3drs375554612
GWAS Ctlgrs375554612
Max Magnitude0
ClinVar
Risk rs375554612(-;-)
Alt rs375554612(-;-)
Reference Rs375554612(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LIG4
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.108861713delT
CLNSRC
CLNACC RCV000480290.1,