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rs606231361

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231361(-;-)
Make rs606231361(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position89007735
GeneFAS
is asnp
is mentioned by
dbSNPrs606231361
ebirs606231361
HLIrs606231361
Exacrs606231361
Varsomers606231361
Maprs606231361
PheGenIrs606231361
hapmaprs606231361
1000 genomesrs606231361
hgdprs606231361
ensemblrs606231361
gopubmedrs606231361
geneviewrs606231361
scholarrs606231361
googlers606231361
pharmgkbrs606231361
gwascentralrs606231361
openSNPrs606231361
23andMers606231361
23andMe allrs606231361
SNP Nexus

SNPshotrs606231361
SNPdbers606231361
MSV3drs606231361
GWAS Ctlgrs606231361
Max Magnitude0
ClinVar
Risk rs606231361(;)
Alt rs606231361(;)
Reference rs606231361(G;G)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90767492delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000017961.29,