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rs796052248

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052248(C;T)
Make rs796052248(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40364964
GeneADSL
is asnp
is mentioned by
dbSNPrs796052248
ebirs796052248
HLIrs796052248
Exacrs796052248
Varsomers796052248
Maprs796052248
PheGenIrs796052248
hapmaprs796052248
1000 genomesrs796052248
hgdprs796052248
ensemblrs796052248
gopubmedrs796052248
geneviewrs796052248
scholarrs796052248
googlers796052248
pharmgkbrs796052248
gwascentralrs796052248
openSNPrs796052248
23andMers796052248
23andMe allrs796052248
SNP Nexus

SNPshotrs796052248
SNPdbers796052248
MSV3drs796052248
GWAS Ctlgrs796052248
Max Magnitude0
ClinVar
Risk rs796052248(T;T)
Alt rs796052248(T;T)
Reference rs796052248(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40760968C>T
CLNSRC
CLNACC RCV000186692.1,