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

rs267607122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607122(C;C)
Make rs267607122(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position89012083
GeneFAS
is asnp
is mentioned by
dbSNPrs267607122
ebirs267607122
HLIrs267607122
Exacrs267607122
Varsomers267607122
Maprs267607122
PheGenIrs267607122
hapmaprs267607122
1000 genomesrs267607122
hgdprs267607122
ensemblrs267607122
gopubmedrs267607122
geneviewrs267607122
scholarrs267607122
googlers267607122
pharmgkbrs267607122
gwascentralrs267607122
openSNPrs267607122
23andMers267607122
23andMe allrs267607122
SNP Nexus

SNPshotrs267607122
SNPdbers267607122
MSV3drs267607122
GWAS Ctlgrs267607122
Max Magnitude0
ClinVar
Risk rs267607122(A,C;A,C)
Alt rs267607122(A,C;A,C)
Reference rs267607122(T;T)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90771840T>A; NC_000010.10:g.90771840T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017971.29, RCV000017978.25,