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rs786205493

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205493(C;T)
Make rs786205493(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position71811978
GeneNR2E3
is asnp
is mentioned by
dbSNPrs786205493
ebirs786205493
HLIrs786205493
Exacrs786205493
Varsomers786205493
Maprs786205493
PheGenIrs786205493
hapmaprs786205493
1000 genomesrs786205493
hgdprs786205493
ensemblrs786205493
gopubmedrs786205493
geneviewrs786205493
scholarrs786205493
googlers786205493
pharmgkbrs786205493
gwascentralrs786205493
openSNPrs786205493
23andMers786205493
23andMe allrs786205493
SNP Nexus

SNPshotrs786205493
SNPdbers786205493
MSV3drs786205493
GWAS Ctlgrs786205493
Max Magnitude0
ClinVar
Risk rs786205493(T;T)
Alt rs786205493(T;T)
Reference rs786205493(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NR2E3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.72104318C>T
CLNSRC
CLNACC RCV000171237.1,