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rs1060499662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499662(C;C)
Make rs1060499662(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position108208948
GeneLIG4
is asnp
is mentioned by
dbSNPrs1060499662
dbSNP (old)rs1060499662
ClinGenrs1060499662
ebirs1060499662
HLIrs1060499662
Exacrs1060499662
Gnomadrs1060499662
Varsomers1060499662
LitVarrs1060499662
Maprs1060499662
PheGenIrs1060499662
Biobankrs1060499662
1000 genomesrs1060499662
hgdprs1060499662
ensemblrs1060499662
gopubmedrs1060499662
geneviewrs1060499662
scholarrs1060499662
googlers1060499662
pharmgkbrs1060499662
gwascentralrs1060499662
openSNPrs1060499662
23andMers1060499662
23andMe allrs1060499662
SNPshotrs1060499662
SNPdbers1060499662
MSV3drs1060499662
GWAS Ctlgrs1060499662
Max Magnitude0
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,