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rs57694264

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs57694264(A;A)
Make rs57694264(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219421517
GeneDES
is asnp
is mentioned by
dbSNPrs57694264
ebirs57694264
HLIrs57694264
Exacrs57694264
Varsomers57694264
Maprs57694264
PheGenIrs57694264
hapmaprs57694264
1000 genomesrs57694264
hgdprs57694264
ensemblrs57694264
gopubmedrs57694264
geneviewrs57694264
scholarrs57694264
googlers57694264
pharmgkbrs57694264
gwascentralrs57694264
openSNPrs57694264
23andMers57694264
23andMe allrs57694264
SNP Nexus

SNPshotrs57694264
SNPdbers57694264
MSV3drs57694264
GWAS Ctlgrs57694264
Max Magnitude0
ClinVar
Risk rs57694264(A;A)
Alt rs57694264(A;A)
Reference rs57694264(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220286239G>A
CLNSRC
CLNACC RCV000056780.2,