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rs606231366

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs606231366(-;-)
Make rs606231366(-;T)
Make rs606231366(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position89014134
GeneFAS
is asnp
is mentioned by
dbSNPrs606231366
ebirs606231366
HLIrs606231366
Exacrs606231366
Varsomers606231366
Maprs606231366
PheGenIrs606231366
hapmaprs606231366
1000 genomesrs606231366
hgdprs606231366
ensemblrs606231366
gopubmedrs606231366
geneviewrs606231366
scholarrs606231366
googlers606231366
pharmgkbrs606231366
gwascentralrs606231366
openSNPrs606231366
23andMers606231366
23andMe allrs606231366
SNP Nexus

SNPshotrs606231366
SNPdbers606231366
MSV3drs606231366
GWAS Ctlgrs606231366
Max Magnitude0
ClinVar
Risk rs606231366(T;T)
Alt rs606231366(T;T)
Reference rs606231366(;)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90773891_90773892insT
CLNSRC OMIM Allelic Variant
CLNACC RCV000017979.29,