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rs104894420

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894420(A;A)
Make rs104894420(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position108209863
GeneLIG4
is asnp
is mentioned by
dbSNPrs104894420
ebirs104894420
HLIrs104894420
Exacrs104894420
Varsomers104894420
Maprs104894420
PheGenIrs104894420
hapmaprs104894420
1000 genomesrs104894420
hgdprs104894420
ensemblrs104894420
gopubmedrs104894420
geneviewrs104894420
scholarrs104894420
googlers104894420
pharmgkbrs104894420
gwascentralrs104894420
openSNPrs104894420
23andMers104894420
23andMe allrs104894420
SNP Nexus

SNPshotrs104894420
SNPdbers104894420
MSV3drs104894420
GWAS Ctlgrs104894420
Max Magnitude0
OMIM601837
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894420(A;A)
Alt rs104894420(A;A)
Reference rs104894420(G;G)
Significance Pathogenic
Disease Lig4 syndrome
Variation info
Gene LIG4
CLNDBN Lig4 syndrome
Reversed 1
HGVS NC_000013.10:g.108862211C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008113.3,