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rs761628767

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761628767(A;A)
Make rs761628767(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position71813567
GeneNR2E3
is asnp
is mentioned by
dbSNPrs761628767
ebirs761628767
HLIrs761628767
Exacrs761628767
Varsomers761628767
Maprs761628767
PheGenIrs761628767
hapmaprs761628767
1000 genomesrs761628767
hgdprs761628767
ensemblrs761628767
gopubmedrs761628767
geneviewrs761628767
scholarrs761628767
googlers761628767
pharmgkbrs761628767
gwascentralrs761628767
openSNPrs761628767
23andMers761628767
23andMe allrs761628767
SNP Nexus

SNPshotrs761628767
SNPdbers761628767
MSV3drs761628767
GWAS Ctlgrs761628767
Max Magnitude0
ClinVar
Risk rs761628767(A,T;A,T)
Alt rs761628767(A,T;A,T)
Reference rs761628767(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NR2E3
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.72105907G>T
CLNSRC
CLNACC RCV000171239.1,