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rs1057521127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521127(A;A)
Make rs1057521127(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position136659069
GeneCD40LG
is asnp
is mentioned by
dbSNPrs1057521127
dbSNP (old)rs1057521127
ClinGenrs1057521127
ebirs1057521127
HLIrs1057521127
Exacrs1057521127
Gnomadrs1057521127
Varsomers1057521127
LitVarrs1057521127
Maprs1057521127
PheGenIrs1057521127
Biobankrs1057521127
1000 genomesrs1057521127
hgdprs1057521127
ensemblrs1057521127
gopubmedrs1057521127
geneviewrs1057521127
scholarrs1057521127
googlers1057521127
pharmgkbrs1057521127
gwascentralrs1057521127
openSNPrs1057521127
23andMers1057521127
23andMe allrs1057521127
SNPshotrs1057521127
SNPdbers1057521127
MSV3drs1057521127
GWAS Ctlgrs1057521127
Max Magnitude0
ClinVar
Risk rs1057521127(A;A)
Alt rs1057521127(A;A)
Reference Rs1057521127(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CD40LG
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135741228C>A
CLNSRC
CLNACC RCV000441734.1,