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rs143083947

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143083947(C;T)
Make rs143083947(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40346563
GeneADSL
is asnp
is mentioned by
dbSNPrs143083947
ebirs143083947
HLIrs143083947
Exacrs143083947
Varsomers143083947
Maprs143083947
PheGenIrs143083947
hapmaprs143083947
1000 genomesrs143083947
hgdprs143083947
ensemblrs143083947
gopubmedrs143083947
geneviewrs143083947
scholarrs143083947
googlers143083947
pharmgkbrs143083947
gwascentralrs143083947
openSNPrs143083947
23andMers143083947
23andMe allrs143083947
SNP Nexus

SNPshotrs143083947
SNPdbers143083947
MSV3drs143083947
GWAS Ctlgrs143083947
Max Magnitude0
ClinVar
Risk rs143083947(T;T)
Alt rs143083947(T;T)
Reference rs143083947(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40742567C>T
CLNSRC
CLNACC RCV000186704.1,