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rs886037777

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs886037777(C;C)
Make rs886037777(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome13
Position108209957
GeneLIG4
is asnp
is mentioned by
dbSNPrs886037777
dbSNP (classic)rs886037777
ClinGenrs886037777
ebirs886037777
HLIrs886037777
Exacrs886037777
Gnomadrs886037777
Varsomers886037777
LitVarrs886037777
Maprs886037777
PheGenIrs886037777
Biobankrs886037777
1000 genomesrs886037777
hgdprs886037777
ensemblrs886037777
geneviewrs886037777
scholarrs886037777
googlers886037777
pharmgkbrs886037777
gwascentralrs886037777
openSNPrs886037777
23andMers886037777
23andMe allrs886037777
SNPshotrs886037777
SNPdbers886037777
MSV3drs886037777
GWAS Ctlgrs886037777
Max Magnitude0
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,