Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776450

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776450(-;-)
Make rs587776450(-;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position172659464
GeneFASLG
is asnp
is mentioned by
dbSNPrs587776450
ebirs587776450
HLIrs587776450
Exacrs587776450
Varsomers587776450
Maprs587776450
PheGenIrs587776450
hapmaprs587776450
1000 genomesrs587776450
hgdprs587776450
ensemblrs587776450
gopubmedrs587776450
geneviewrs587776450
scholarrs587776450
googlers587776450
pharmgkbrs587776450
gwascentralrs587776450
openSNPrs587776450
23andMers587776450
23andMe allrs587776450
SNP Nexus

SNPshotrs587776450
SNPdbers587776450
MSV3drs587776450
GWAS Ctlgrs587776450
Max Magnitude0
ClinVar
Risk rs587776450(;)
Alt rs587776450(;)
Reference rs587776450(T;T)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FASLG
CLNDBN Autoimmune lymphoproliferative syndrome
Reversed 0
HGVS NC_000001.10:g.172628604delT
CLNSRC ClinVar
CLNACC RCV000144151.1,