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rs200862792

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200862792(A;A)
Make rs200862792(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74056402
GeneELN
is asnp
is mentioned by
dbSNPrs200862792
ebirs200862792
HLIrs200862792
Exacrs200862792
Varsomers200862792
Maprs200862792
PheGenIrs200862792
hapmaprs200862792
1000 genomesrs200862792
hgdprs200862792
ensemblrs200862792
gopubmedrs200862792
geneviewrs200862792
scholarrs200862792
googlers200862792
pharmgkbrs200862792
gwascentralrs200862792
openSNPrs200862792
23andMers200862792
23andMe allrs200862792
SNP Nexus

SNPshotrs200862792
SNPdbers200862792
MSV3drs200862792
GWAS Ctlgrs200862792
Max Magnitude0
ClinVar
Risk rs200862792(A,T;A,T)
Alt rs200862792(A,T;A,T)
Reference rs200862792(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73470732G>T
CLNSRC
CLNACC RCV000196367.1,