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rs794729087

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729087(A;A)
Make rs794729087(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position77942801
GeneNEXN
is asnp
is mentioned by
dbSNPrs794729087
ebirs794729087
HLIrs794729087
Exacrs794729087
Varsomers794729087
Maprs794729087
PheGenIrs794729087
hapmaprs794729087
1000 genomesrs794729087
hgdprs794729087
ensemblrs794729087
gopubmedrs794729087
geneviewrs794729087
scholarrs794729087
googlers794729087
pharmgkbrs794729087
gwascentralrs794729087
openSNPrs794729087
23andMers794729087
23andMe allrs794729087
SNP Nexus

SNPshotrs794729087
SNPdbers794729087
MSV3drs794729087
GWAS Ctlgrs794729087
Max Magnitude0
ClinVar
Risk rs794729087(A;A)
Alt rs794729087(A;A)
Reference rs794729087(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEXN
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.78408486G>A
CLNSRC
CLNACC RCV000183675.2,