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

rs121918660

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918660(A;A)
Make rs121918660(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position86790400
GeneCD8A
is asnp
is mentioned by
dbSNPrs121918660
ebirs121918660
HLIrs121918660
Exacrs121918660
Varsomers121918660
Maprs121918660
PheGenIrs121918660
hapmaprs121918660
1000 genomesrs121918660
hgdprs121918660
ensemblrs121918660
gopubmedrs121918660
geneviewrs121918660
scholarrs121918660
googlers121918660
pharmgkbrs121918660
gwascentralrs121918660
openSNPrs121918660
23andMers121918660
23andMe allrs121918660
SNP Nexus

SNPshotrs121918660
SNPdbers121918660
MSV3drs121918660
GWAS Ctlgrs121918660
Max Magnitude0
OMIM186910
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918660(A;A)
Alt rs121918660(A;A)
Reference rs121918660(G;G)
Significance Pathogenic
Disease Cd8 deficiency
Variation info
Gene CD8A
CLNDBN Cd8 deficiency, familial
Reversed 1
HGVS NC_000002.11:g.87017523C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013579.23,