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rs61726467

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61726467(A;A)
Make rs61726467(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219421553
GeneDES
is asnp
is mentioned by
dbSNPrs61726467
ebirs61726467
HLIrs61726467
Exacrs61726467
Varsomers61726467
Maprs61726467
PheGenIrs61726467
hapmaprs61726467
1000 genomesrs61726467
hgdprs61726467
ensemblrs61726467
gopubmedrs61726467
geneviewrs61726467
scholarrs61726467
googlers61726467
pharmgkbrs61726467
gwascentralrs61726467
openSNPrs61726467
23andMers61726467
23andMe allrs61726467
SNP Nexus

SNPshotrs61726467
SNPdbers61726467
MSV3drs61726467
GWAS Ctlgrs61726467
Max Magnitude0
ClinVar
Risk rs61726467(A;A)
Alt rs61726467(A;A)
Reference rs61726467(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220286275G>A
CLNSRC
CLNACC RCV000056782.3,