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rs1057521795

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521795(C;C)
Make rs1057521795(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position40366481
GeneADSL
is asnp
is mentioned by
dbSNPrs1057521795
dbSNP (old)rs1057521795
ClinGenrs1057521795
ebirs1057521795
HLIrs1057521795
Exacrs1057521795
Gnomadrs1057521795
Varsomers1057521795
Maprs1057521795
PheGenIrs1057521795
Biobankrs1057521795
1000 genomesrs1057521795
hgdprs1057521795
ensemblrs1057521795
gopubmedrs1057521795
geneviewrs1057521795
scholarrs1057521795
googlers1057521795
pharmgkbrs1057521795
gwascentralrs1057521795
openSNPrs1057521795
23andMers1057521795
23andMe allrs1057521795
SNPshotrs1057521795
SNPdbers1057521795
MSV3drs1057521795
GWAS Ctlgrs1057521795
Max Magnitude0
ClinVar
Risk rs1057521795(C;C)
Alt rs1057521795(C;C)
Reference Rs1057521795(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADSL
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.40762485T>C
CLNSRC
CLNACC RCV000442330.1,