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rs1036185928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1036185928(C;T)
Make rs1036185928(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position40349931
GeneADSL
is asnp
is mentioned by
dbSNPrs1036185928
dbSNP (old)rs1036185928
ClinGenrs1036185928
ebirs1036185928
HLIrs1036185928
Exacrs1036185928
Gnomadrs1036185928
Varsomers1036185928
LitVarrs1036185928
Maprs1036185928
PheGenIrs1036185928
Biobankrs1036185928
1000 genomesrs1036185928
hgdprs1036185928
ensemblrs1036185928
gopubmedrs1036185928
geneviewrs1036185928
scholarrs1036185928
googlers1036185928
pharmgkbrs1036185928
gwascentralrs1036185928
openSNPrs1036185928
23andMers1036185928
23andMe allrs1036185928
SNPshotrs1036185928
SNPdbers1036185928
MSV3drs1036185928
GWAS Ctlgrs1036185928
Max Magnitude0
ClinVar
Risk rs1036185928(T;T)
Alt rs1036185928(T;T)
Reference Rs1036185928(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40745935C>T
CLNSRC
CLNACC RCV000434653.1,