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rs527441189

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527441189(A;A)
Make rs527441189(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74051764
GeneELN
is asnp
is mentioned by
dbSNPrs527441189
ebirs527441189
HLIrs527441189
Exacrs527441189
Varsomers527441189
Maprs527441189
PheGenIrs527441189
hapmaprs527441189
1000 genomesrs527441189
hgdprs527441189
ensemblrs527441189
gopubmedrs527441189
geneviewrs527441189
scholarrs527441189
googlers527441189
pharmgkbrs527441189
gwascentralrs527441189
openSNPrs527441189
23andMers527441189
23andMe allrs527441189
SNP Nexus

SNPshotrs527441189
SNPdbers527441189
MSV3drs527441189
GWAS Ctlgrs527441189
Max Magnitude0
ClinVar
Risk rs527441189(A;A)
Alt rs527441189(A;A)
Reference rs527441189(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73466094G>T
CLNSRC
CLNACC RCV000196542.1,