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

rs606231305

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231305(A;A)
Make rs606231305(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position85276295
GeneBCL10, LOC646626
is asnp
is mentioned by
dbSNPrs606231305
ebirs606231305
HLIrs606231305
Exacrs606231305
Varsomers606231305
Maprs606231305
PheGenIrs606231305
hapmaprs606231305
1000 genomesrs606231305
hgdprs606231305
ensemblrs606231305
gopubmedrs606231305
geneviewrs606231305
scholarrs606231305
googlers606231305
pharmgkbrs606231305
gwascentralrs606231305
openSNPrs606231305
23andMers606231305
23andMe allrs606231305
SNP Nexus

SNPshotrs606231305
SNPdbers606231305
MSV3drs606231305
GWAS Ctlgrs606231305
Max Magnitude0
ClinVar
Risk rs606231305(A;A)
Alt rs606231305(A;A)
Reference rs606231305(G;G)
Significance Pathogenic
Disease Immunodeficiency 37
Variation info
Gene BCL10 LOC646626
CLNDBN Immunodeficiency 37
Reversed 1
HGVS NC_000001.10:g.85741978C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000148013.3,