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rs201176444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201176444(A;A)
Make rs201176444(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position108208685
GeneLIG4
is asnp
is mentioned by
dbSNPrs201176444
dbSNP (classic)rs201176444
ClinGenrs201176444
ebirs201176444
HLIrs201176444
Exacrs201176444
Gnomadrs201176444
Varsomers201176444
LitVarrs201176444
Maprs201176444
PheGenIrs201176444
Biobankrs201176444
1000 genomesrs201176444
hgdprs201176444
ensemblrs201176444
geneviewrs201176444
scholarrs201176444
googlers201176444
pharmgkbrs201176444
gwascentralrs201176444
openSNPrs201176444
23andMers201176444
23andMe allrs201176444
SNPshotrs201176444
SNPdbers201176444
MSV3drs201176444
GWAS Ctlgrs201176444
Max Magnitude0
ClinVar
Risk rs201176444(A;A)
Alt rs201176444(A;A)
Reference Rs201176444(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LIG4
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.108861033G>A
CLNSRC
CLNACC RCV000485558.1,