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rs796052247

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052247(C;C)
Make rs796052247(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40364302
GeneADSL
is asnp
is mentioned by
dbSNPrs796052247
ebirs796052247
HLIrs796052247
Exacrs796052247
Varsomers796052247
Maprs796052247
PheGenIrs796052247
hapmaprs796052247
1000 genomesrs796052247
hgdprs796052247
ensemblrs796052247
gopubmedrs796052247
geneviewrs796052247
scholarrs796052247
googlers796052247
pharmgkbrs796052247
gwascentralrs796052247
openSNPrs796052247
23andMers796052247
23andMe allrs796052247
SNP Nexus

SNPshotrs796052247
SNPdbers796052247
MSV3drs796052247
GWAS Ctlgrs796052247
Max Magnitude0
ClinVar
Risk rs796052247(C;C)
Alt rs796052247(C;C)
Reference rs796052247(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40760306G>C
CLNSRC
CLNACC RCV000186689.1,