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rs761242509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761242509(C;T)
Make rs761242509(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome20
Position44625568
GeneADA
is asnp
is mentioned by
dbSNPrs761242509
dbSNP (classic)rs761242509
ClinGenrs761242509
ebirs761242509
HLIrs761242509
Exacrs761242509
Gnomadrs761242509
Varsomers761242509
LitVarrs761242509
Maprs761242509
PheGenIrs761242509
Biobankrs761242509
1000 genomesrs761242509
hgdprs761242509
ensemblrs761242509
geneviewrs761242509
scholarrs761242509
googlers761242509
pharmgkbrs761242509
gwascentralrs761242509
openSNPrs761242509
23andMers761242509
23andMe allrs761242509
SNPshotrs761242509
SNPdbers761242509
MSV3drs761242509
GWAS Ctlgrs761242509
Max Magnitude0
ClinVar
Risk rs761242509(T;T)
Alt rs761242509(T;T)
Reference Rs761242509(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADA
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.43254209C>T
CLNSRC
CLNACC RCV000254941.1,