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rs1057521128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521128(C;C)
Make rs1057521128(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position136659396
GeneCD40LG
is asnp
is mentioned by
dbSNPrs1057521128
dbSNP (classic)rs1057521128
ClinGenrs1057521128
ebirs1057521128
HLIrs1057521128
Exacrs1057521128
Gnomadrs1057521128
Varsomers1057521128
LitVarrs1057521128
Maprs1057521128
PheGenIrs1057521128
Biobankrs1057521128
1000 genomesrs1057521128
hgdprs1057521128
ensemblrs1057521128
geneviewrs1057521128
scholarrs1057521128
googlers1057521128
pharmgkbrs1057521128
gwascentralrs1057521128
openSNPrs1057521128
23andMers1057521128
23andMe allrs1057521128
SNPshotrs1057521128
SNPdbers1057521128
MSV3drs1057521128
GWAS Ctlgrs1057521128
Max Magnitude0
ClinVar
Risk rs1057521128(C;C)
Alt rs1057521128(C;C)
Reference Rs1057521128(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CD40LG
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135741555T>C
CLNSRC
CLNACC RCV000423996.1,