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rs794729086

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729086(C;G)
Make rs794729086(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position77942736
GeneNEXN
is asnp
is mentioned by
dbSNPrs794729086
ebirs794729086
HLIrs794729086
Exacrs794729086
Varsomers794729086
Maprs794729086
PheGenIrs794729086
hapmaprs794729086
1000 genomesrs794729086
hgdprs794729086
ensemblrs794729086
gopubmedrs794729086
geneviewrs794729086
scholarrs794729086
googlers794729086
pharmgkbrs794729086
gwascentralrs794729086
openSNPrs794729086
23andMers794729086
23andMe allrs794729086
SNP Nexus

SNPshotrs794729086
SNPdbers794729086
MSV3drs794729086
GWAS Ctlgrs794729086
Max Magnitude0
ClinVar
Risk rs794729086(G;G)
Alt rs794729086(G;G)
Reference rs794729086(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene NEXN
CLNDBN not provided not specified
Reversed 0
HGVS NC_000001.10:g.78408421C>G
CLNSRC
CLNACC RCV000183673.1, RCV000223684.1,