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rs771121666

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs771121666(C;C)
Make rs771121666(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40365030
GeneADSL
is asnp
is mentioned by
dbSNPrs771121666
ebirs771121666
HLIrs771121666
Exacrs771121666
Varsomers771121666
Maprs771121666
PheGenIrs771121666
hapmaprs771121666
1000 genomesrs771121666
hgdprs771121666
ensemblrs771121666
gopubmedrs771121666
geneviewrs771121666
scholarrs771121666
googlers771121666
pharmgkbrs771121666
gwascentralrs771121666
openSNPrs771121666
23andMers771121666
23andMe allrs771121666
SNP Nexus

SNPshotrs771121666
SNPdbers771121666
MSV3drs771121666
GWAS Ctlgrs771121666
Max Magnitude0
ClinVar
Risk rs771121666(C;C)
Alt rs771121666(C;C)
Reference rs771121666(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40761034T>C
CLNSRC
CLNACC RCV000224729.1,