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rs1057520217

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520217(C;T)
Make rs1057520217(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position44651601
GeneADA
is asnp
is mentioned by
dbSNPrs1057520217
dbSNP (old)rs1057520217
ClinGenrs1057520217
ebirs1057520217
HLIrs1057520217
Exacrs1057520217
Gnomadrs1057520217
Varsomers1057520217
Maprs1057520217
PheGenIrs1057520217
Biobankrs1057520217
1000 genomesrs1057520217
hgdprs1057520217
ensemblrs1057520217
gopubmedrs1057520217
geneviewrs1057520217
scholarrs1057520217
googlers1057520217
pharmgkbrs1057520217
gwascentralrs1057520217
openSNPrs1057520217
23andMers1057520217
23andMe allrs1057520217
SNPshotrs1057520217
SNPdbers1057520217
MSV3drs1057520217
GWAS Ctlgrs1057520217
Max Magnitude0
ClinVar
Risk rs1057520217(T;T)
Alt rs1057520217(T;T)
Reference Rs1057520217(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADA
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.43280242G>A
CLNSRC
CLNACC RCV000433743.1,