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rs1057523274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523274(A;G)
Make rs1057523274(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position219418463
GeneDES
is asnp
is mentioned by
dbSNPrs1057523274
dbSNP (classic)rs1057523274
ClinGenrs1057523274
ebirs1057523274
HLIrs1057523274
Exacrs1057523274
Gnomadrs1057523274
Varsomers1057523274
LitVarrs1057523274
Maprs1057523274
PheGenIrs1057523274
Biobankrs1057523274
1000 genomesrs1057523274
hgdprs1057523274
ensemblrs1057523274
geneviewrs1057523274
scholarrs1057523274
googlers1057523274
pharmgkbrs1057523274
gwascentralrs1057523274
openSNPrs1057523274
23andMers1057523274
23andMe allrs1057523274
SNPshotrs1057523274
SNPdbers1057523274
MSV3drs1057523274
GWAS Ctlgrs1057523274
Max Magnitude0
ClinVar
Risk rs1057523274(G;G)
Alt rs1057523274(G;G)
Reference Rs1057523274(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220283185A>G
CLNSRC
CLNACC RCV000417495.1,