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rs606231364

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231364(A;A)
Make rs606231364(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position89003071
GeneFAS, LOC105378417
is asnp
is mentioned by
dbSNPrs606231364
ebirs606231364
HLIrs606231364
Exacrs606231364
Varsomers606231364
Maprs606231364
PheGenIrs606231364
hapmaprs606231364
1000 genomesrs606231364
hgdprs606231364
ensemblrs606231364
gopubmedrs606231364
geneviewrs606231364
scholarrs606231364
googlers606231364
pharmgkbrs606231364
gwascentralrs606231364
openSNPrs606231364
23andMers606231364
23andMe allrs606231364
SNP Nexus

SNPshotrs606231364
SNPdbers606231364
MSV3drs606231364
GWAS Ctlgrs606231364
Max Magnitude0
ClinVar
Risk rs606231364(A;A)
Alt rs606231364(A;A)
Reference rs606231364(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.90762828G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017972.25,