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rs1057518628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518628(-;-)
Make rs1057518628(-;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position136659107
GeneCD40LG
is asnp
is mentioned by
dbSNPrs1057518628
dbSNP (old)rs1057518628
ClinGenrs1057518628
ebirs1057518628
HLIrs1057518628
Exacrs1057518628
Gnomadrs1057518628
Varsomers1057518628
Maprs1057518628
PheGenIrs1057518628
Biobankrs1057518628
1000 genomesrs1057518628
hgdprs1057518628
ensemblrs1057518628
gopubmedrs1057518628
geneviewrs1057518628
scholarrs1057518628
googlers1057518628
pharmgkbrs1057518628
gwascentralrs1057518628
openSNPrs1057518628
23andMers1057518628
23andMe allrs1057518628
SNPshotrs1057518628
SNPdbers1057518628
MSV3drs1057518628
GWAS Ctlgrs1057518628
Max Magnitude0
ClinVar
Risk rs1057518628(-;-)
Alt rs1057518628(-;-)
Reference Rs1057518628(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CD40LG
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135741266delC
CLNSRC
CLNACC RCV000414255.1,