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rs1057520275

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520275(A;A)
Make rs1057520275(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position219421533
GeneDES
is asnp
is mentioned by
dbSNPrs1057520275
dbSNP (old)rs1057520275
ClinGenrs1057520275
ebirs1057520275
HLIrs1057520275
Exacrs1057520275
Gnomadrs1057520275
Varsomers1057520275
Maprs1057520275
PheGenIrs1057520275
Biobankrs1057520275
1000 genomesrs1057520275
hgdprs1057520275
ensemblrs1057520275
gopubmedrs1057520275
geneviewrs1057520275
scholarrs1057520275
googlers1057520275
pharmgkbrs1057520275
gwascentralrs1057520275
openSNPrs1057520275
23andMers1057520275
23andMe allrs1057520275
SNPshotrs1057520275
SNPdbers1057520275
MSV3drs1057520275
GWAS Ctlgrs1057520275
Max Magnitude0
ClinVar
Risk rs1057520275(A;A)
Alt rs1057520275(A;A)
Reference Rs1057520275(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220286255G>A
CLNSRC
CLNACC RCV000437250.1,