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rs267607498

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607498(A;G)
Make rs267607498(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219425707
GeneDES
is asnp
is mentioned by
dbSNPrs267607498
ebirs267607498
HLIrs267607498
Exacrs267607498
Varsomers267607498
Maprs267607498
PheGenIrs267607498
hapmaprs267607498
1000 genomesrs267607498
hgdprs267607498
ensemblrs267607498
gopubmedrs267607498
geneviewrs267607498
scholarrs267607498
googlers267607498
pharmgkbrs267607498
gwascentralrs267607498
openSNPrs267607498
23andMers267607498
23andMe allrs267607498
SNP Nexus

SNPshotrs267607498
SNPdbers267607498
MSV3drs267607498
GWAS Ctlgrs267607498
Max Magnitude0
ClinVar
Risk rs267607498(G;G)
Alt rs267607498(G;G)
Reference rs267607498(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene DES LOC101928568
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220290429A>G
CLNSRC
CLNACC RCV000056785.2,