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rs372895468

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372895468(C;T)
Make rs372895468(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40365037
GeneADSL
is asnp
is mentioned by
dbSNPrs372895468
ebirs372895468
HLIrs372895468
Exacrs372895468
Varsomers372895468
Maprs372895468
PheGenIrs372895468
hapmaprs372895468
1000 genomesrs372895468
hgdprs372895468
ensemblrs372895468
gopubmedrs372895468
geneviewrs372895468
scholarrs372895468
googlers372895468
pharmgkbrs372895468
gwascentralrs372895468
openSNPrs372895468
23andMers372895468
23andMe allrs372895468
SNP Nexus

SNPshotrs372895468
SNPdbers372895468
MSV3drs372895468
GWAS Ctlgrs372895468
Max Magnitude0
ClinVar
Risk rs372895468(G,T;G,T)
Alt rs372895468(G,T;G,T)
Reference rs372895468(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40761041C>G
CLNSRC
CLNACC RCV000186712.1,