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rs772226399

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCTTT;TCTTT) 0 common in clinvar
Make rs772226399(-;-)
Make rs772226399(-;TCTTT)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position108209994
GeneLIG4
is asnp
is mentioned by
dbSNPrs772226399
dbSNP (classic)rs772226399
ClinGenrs772226399
ebirs772226399
HLIrs772226399
Exacrs772226399
Gnomadrs772226399
Varsomers772226399
LitVarrs772226399
Maprs772226399
PheGenIrs772226399
Biobankrs772226399
1000 genomesrs772226399
hgdprs772226399
ensemblrs772226399
geneviewrs772226399
scholarrs772226399
googlers772226399
pharmgkbrs772226399
gwascentralrs772226399
openSNPrs772226399
23andMers772226399
23andMe allrs772226399
SNPshotrs772226399
SNPdbers772226399
MSV3drs772226399
GWAS Ctlgrs772226399
Max Magnitude0
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,