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

rs606231363

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs606231363(A;C)
Make rs606231363(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position89011997
GeneFAS
is asnp
is mentioned by
dbSNPrs606231363
ebirs606231363
HLIrs606231363
Exacrs606231363
Varsomers606231363
Maprs606231363
PheGenIrs606231363
hapmaprs606231363
1000 genomesrs606231363
hgdprs606231363
ensemblrs606231363
gopubmedrs606231363
geneviewrs606231363
scholarrs606231363
googlers606231363
pharmgkbrs606231363
gwascentralrs606231363
openSNPrs606231363
23andMers606231363
23andMe allrs606231363
SNP Nexus

SNPshotrs606231363
SNPdbers606231363
MSV3drs606231363
GWAS Ctlgrs606231363
Max Magnitude0
ClinVar
Risk rs606231363(C;C)
Alt rs606231363(C;C)
Reference rs606231363(A;A)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90771754A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017964.29,