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rs1057524203

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524203(C;T)
Make rs1057524203(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position56615924
GeneDST
is asnp
is mentioned by
dbSNPrs1057524203
dbSNP (old)rs1057524203
ClinGenrs1057524203
ebirs1057524203
HLIrs1057524203
Exacrs1057524203
Gnomadrs1057524203
Varsomers1057524203
LitVarrs1057524203
Maprs1057524203
PheGenIrs1057524203
Biobankrs1057524203
1000 genomesrs1057524203
hgdprs1057524203
ensemblrs1057524203
gopubmedrs1057524203
geneviewrs1057524203
scholarrs1057524203
googlers1057524203
pharmgkbrs1057524203
gwascentralrs1057524203
openSNPrs1057524203
23andMers1057524203
23andMe allrs1057524203
SNPshotrs1057524203
SNPdbers1057524203
MSV3drs1057524203
GWAS Ctlgrs1057524203
Max Magnitude0
ClinVar
Risk rs1057524203(T;T)
Alt rs1057524203(T;T)
Reference Rs1057524203(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DST
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.56480722G>A
CLNSRC
CLNACC RCV000430694.1,