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rs121908156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908156(C;T)
Make rs121908156(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position14945110
GeneDCLRE1C
is asnp
is mentioned by
dbSNPrs121908156
ebirs121908156
HLIrs121908156
Exacrs121908156
Varsomers121908156
Maprs121908156
PheGenIrs121908156
hapmaprs121908156
1000 genomesrs121908156
hgdprs121908156
ensemblrs121908156
gopubmedrs121908156
geneviewrs121908156
scholarrs121908156
googlers121908156
pharmgkbrs121908156
gwascentralrs121908156
openSNPrs121908156
23andMers121908156
23andMe allrs121908156
SNP Nexus

SNPshotrs121908156
SNPdbers121908156
MSV3drs121908156
GWAS Ctlgrs121908156
Max Magnitude0
OMIM605988
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908156(A,T;A,T)
Alt rs121908156(A,T;A,T)
Reference rs121908156(C;C)
Significance Pathogenic
Disease Severe combined immunodeficiency with sensitivity to ionizing radiation not provided
Variation info
Gene DCLRE1C
CLNDBN Severe combined immunodeficiency with sensitivity to ionizing radiation not provided
Reversed 1
HGVS NC_000010.10:g.14987109G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004929.3, RCV000224235.1,