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rs786205074

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205074(-;-)
Make rs786205074(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position14932854
GeneDCLRE1C
is asnp
is mentioned by
dbSNPrs786205074
ebirs786205074
HLIrs786205074
Exacrs786205074
Varsomers786205074
Maprs786205074
PheGenIrs786205074
hapmaprs786205074
1000 genomesrs786205074
hgdprs786205074
ensemblrs786205074
gopubmedrs786205074
geneviewrs786205074
scholarrs786205074
googlers786205074
pharmgkbrs786205074
gwascentralrs786205074
openSNPrs786205074
23andMers786205074
23andMe allrs786205074
SNP Nexus

SNPshotrs786205074
SNPdbers786205074
MSV3drs786205074
GWAS Ctlgrs786205074
Max Magnitude0
ClinVar
Risk rs786205074(;)
Alt rs786205074(;)
Reference rs786205074(G;G)
Significance Pathogenic
Disease Severe combined immunodeficiency with sensitivity to ionizing radiation
Variation info
Gene DCLRE1C
CLNDBN Severe combined immunodeficiency with sensitivity to ionizing radiation
Reversed 1
HGVS NC_000010.10:g.14974853delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000004935.3,