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rs1057521071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521071(C;G)
Make rs1057521071(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position40366467
GeneADSL
is asnp
is mentioned by
dbSNPrs1057521071
dbSNP (old)rs1057521071
ClinGenrs1057521071
ebirs1057521071
HLIrs1057521071
Exacrs1057521071
Gnomadrs1057521071
Varsomers1057521071
Maprs1057521071
PheGenIrs1057521071
Biobankrs1057521071
1000 genomesrs1057521071
hgdprs1057521071
ensemblrs1057521071
gopubmedrs1057521071
geneviewrs1057521071
scholarrs1057521071
googlers1057521071
pharmgkbrs1057521071
gwascentralrs1057521071
openSNPrs1057521071
23andMers1057521071
23andMe allrs1057521071
SNPshotrs1057521071
SNPdbers1057521071
MSV3drs1057521071
GWAS Ctlgrs1057521071
Max Magnitude0
ClinVar
Risk rs1057521071(G;G)
Alt rs1057521071(G;G)
Reference Rs1057521071(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40762471C>G
CLNSRC
CLNACC RCV000438014.1,