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rs771266745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTCTT;CTCTT) 0 common in clinvar
Make rs771266745(-;-)
Make rs771266745(-;TTCTC)
Make rs771266745(TTCTC;TTCTC)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position44621033
GeneADA
is asnp
is mentioned by
dbSNPrs771266745
dbSNP (old)rs771266745
ClinGenrs771266745
ebirs771266745
HLIrs771266745
Exacrs771266745
Gnomadrs771266745
Varsomers771266745
Maprs771266745
PheGenIrs771266745
Biobankrs771266745
1000 genomesrs771266745
hgdprs771266745
ensemblrs771266745
gopubmedrs771266745
geneviewrs771266745
scholarrs771266745
googlers771266745
pharmgkbrs771266745
gwascentralrs771266745
openSNPrs771266745
23andMers771266745
23andMe allrs771266745
SNP Nexus

SNPshotrs771266745
SNPdbers771266745
MSV3drs771266745
GWAS Ctlgrs771266745
Max Magnitude0
ClinVar
Risk rs771266745(-;-)
Alt rs771266745(-;-)
Reference Rs771266745(CTCTT;CTCTT)
Significance Other
Disease Severe combined immunodeficiency due to ADA deficiency not provided
Variation info
Gene ADA
CLNDBN Severe combined immunodeficiency due to ADA deficiency not provided
Reversed 0
HGVS NC_000020.10:g.43249674_43249678delCTCTT
CLNSRC
CLNACC RCV000173618.1, RCV000255208.1,