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rs606231362

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs606231362(-;-)
Make rs606231362(-;T)
Make rs606231362(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position89007839
GeneFAS
is asnp
is mentioned by
dbSNPrs606231362
ebirs606231362
HLIrs606231362
Exacrs606231362
Varsomers606231362
Maprs606231362
PheGenIrs606231362
hapmaprs606231362
1000 genomesrs606231362
hgdprs606231362
ensemblrs606231362
gopubmedrs606231362
geneviewrs606231362
scholarrs606231362
googlers606231362
pharmgkbrs606231362
gwascentralrs606231362
openSNPrs606231362
23andMers606231362
23andMe allrs606231362
SNP Nexus

SNPshotrs606231362
SNPdbers606231362
MSV3drs606231362
GWAS Ctlgrs606231362
Max Magnitude0
ClinVar
Risk rs606231362(T;T)
Alt rs606231362(T;T)
Reference rs606231362(;)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90767596dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000017962.25,