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rs786205607

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs786205607(-;-)
Make rs786205607(-;AT)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position136659348
GeneCD40LG
is asnp
is mentioned by
dbSNPrs786205607
ebirs786205607
HLIrs786205607
Exacrs786205607
Varsomers786205607
Maprs786205607
PheGenIrs786205607
hapmaprs786205607
1000 genomesrs786205607
hgdprs786205607
ensemblrs786205607
gopubmedrs786205607
geneviewrs786205607
scholarrs786205607
googlers786205607
pharmgkbrs786205607
gwascentralrs786205607
openSNPrs786205607
23andMers786205607
23andMe allrs786205607
SNP Nexus

SNPshotrs786205607
SNPdbers786205607
MSV3drs786205607
GWAS Ctlgrs786205607
Max Magnitude0
ClinVar
Risk rs786205607(;)
Alt rs786205607(;)
Reference rs786205607(AT;AT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CD40LG
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135741507_135741508delAT
CLNSRC
CLNACC RCV000171445.1,