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rs763903197

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763903197(A;A)
Make rs763903197(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position219421343
GeneDES
is asnp
is mentioned by
dbSNPrs763903197
ebirs763903197
HLIrs763903197
Exacrs763903197
Varsomers763903197
Maprs763903197
PheGenIrs763903197
hapmaprs763903197
1000 genomesrs763903197
hgdprs763903197
ensemblrs763903197
gopubmedrs763903197
geneviewrs763903197
scholarrs763903197
googlers763903197
pharmgkbrs763903197
gwascentralrs763903197
openSNPrs763903197
23andMers763903197
23andMe allrs763903197
SNP Nexus

SNPshotrs763903197
SNPdbers763903197
MSV3drs763903197
GWAS Ctlgrs763903197
Max Magnitude0
ClinVar
Risk rs763903197(A;A)
Alt rs763903197(A;A)
Reference rs763903197(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DES
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.220286065G>A
CLNSRC
CLNACC RCV000183353.2,