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rs761493155

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761493155(C;T)
Make rs761493155(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40361634
GeneADSL
is asnp
is mentioned by
dbSNPrs761493155
ebirs761493155
HLIrs761493155
Exacrs761493155
Varsomers761493155
Maprs761493155
PheGenIrs761493155
hapmaprs761493155
1000 genomesrs761493155
hgdprs761493155
ensemblrs761493155
gopubmedrs761493155
geneviewrs761493155
scholarrs761493155
googlers761493155
pharmgkbrs761493155
gwascentralrs761493155
openSNPrs761493155
23andMers761493155
23andMe allrs761493155
SNP Nexus

SNPshotrs761493155
SNPdbers761493155
MSV3drs761493155
GWAS Ctlgrs761493155
Max Magnitude0
ClinVar
Risk rs761493155(T;T)
Alt rs761493155(T;T)
Reference rs761493155(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40757638C>T
CLNSRC
CLNACC RCV000186680.1,