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rs786205606

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205606(A;G)
Make rs786205606(G;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position136659135
GeneCD40LG
is asnp
is mentioned by
dbSNPrs786205606
ebirs786205606
HLIrs786205606
Exacrs786205606
Varsomers786205606
Maprs786205606
PheGenIrs786205606
hapmaprs786205606
1000 genomesrs786205606
hgdprs786205606
ensemblrs786205606
gopubmedrs786205606
geneviewrs786205606
scholarrs786205606
googlers786205606
pharmgkbrs786205606
gwascentralrs786205606
openSNPrs786205606
23andMers786205606
23andMe allrs786205606
SNP Nexus

SNPshotrs786205606
SNPdbers786205606
MSV3drs786205606
GWAS Ctlgrs786205606
Max Magnitude0
ClinVar
Risk rs786205606(G;G)
Alt rs786205606(G;G)
Reference rs786205606(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CD40LG
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135741294A>G
CLNSRC
CLNACC RCV000171444.1,