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rs368098126

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368098126(A;A)
Make rs368098126(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position71812410
GeneNR2E3
is asnp
is mentioned by
dbSNPrs368098126
ebirs368098126
HLIrs368098126
Exacrs368098126
Varsomers368098126
Maprs368098126
PheGenIrs368098126
hapmaprs368098126
1000 genomesrs368098126
hgdprs368098126
ensemblrs368098126
gopubmedrs368098126
geneviewrs368098126
scholarrs368098126
googlers368098126
pharmgkbrs368098126
gwascentralrs368098126
openSNPrs368098126
23andMers368098126
23andMe allrs368098126
SNP Nexus

SNPshotrs368098126
SNPdbers368098126
MSV3drs368098126
GWAS Ctlgrs368098126
Max Magnitude0
ClinVar
Risk rs368098126(A;A)
Alt rs368098126(A;A)
Reference rs368098126(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NR2E3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.72104750G>A
CLNSRC
CLNACC RCV000171238.1,