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rs777821034

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs777821034(C;C)
Make rs777821034(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position40365027
GeneADSL
is asnp
is mentioned by
dbSNPrs777821034
ebirs777821034
HLIrs777821034
Exacrs777821034
Varsomers777821034
Maprs777821034
PheGenIrs777821034
hapmaprs777821034
1000 genomesrs777821034
hgdprs777821034
ensemblrs777821034
gopubmedrs777821034
geneviewrs777821034
scholarrs777821034
googlers777821034
pharmgkbrs777821034
gwascentralrs777821034
openSNPrs777821034
23andMers777821034
23andMe allrs777821034
SNP Nexus

SNPshotrs777821034
SNPdbers777821034
MSV3drs777821034
GWAS Ctlgrs777821034
Max Magnitude0
ClinVar
Risk rs777821034(C;C)
Alt rs777821034(C;C)
Reference rs777821034(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40761031T>C
CLNSRC
CLNACC RCV000186696.2,