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rs763595926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCAC;TCAC) 0 common in clinvar
Make rs763595926(-;-)
Make rs763595926(-;TCAC)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position44626448
GeneADA
is asnp
is mentioned by
dbSNPrs763595926
dbSNP (classic)rs763595926
ClinGenrs763595926
ebirs763595926
HLIrs763595926
Exacrs763595926
Gnomadrs763595926
Varsomers763595926
LitVarrs763595926
Maprs763595926
PheGenIrs763595926
Biobankrs763595926
1000 genomesrs763595926
hgdprs763595926
ensemblrs763595926
geneviewrs763595926
scholarrs763595926
googlers763595926
pharmgkbrs763595926
gwascentralrs763595926
openSNPrs763595926
23andMers763595926
23andMe allrs763595926
SNPshotrs763595926
SNPdbers763595926
MSV3drs763595926
GWAS Ctlgrs763595926
Max Magnitude0
ClinVar
Risk rs763595926(-;-)
Alt rs763595926(-;-)
Reference Rs763595926(TCAC;TCAC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADA
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.43255089_43255092delTCAC
CLNSRC
CLNACC RCV000481952.1,