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rs794729092

From SNPedia

Orientationplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs794729092(-;-)
Make rs794729092(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position77936016
GeneNEXN
is asnp
is mentioned by
dbSNPrs794729092
ebirs794729092
HLIrs794729092
Exacrs794729092
Varsomers794729092
Maprs794729092
PheGenIrs794729092
hapmaprs794729092
1000 genomesrs794729092
hgdprs794729092
ensemblrs794729092
gopubmedrs794729092
geneviewrs794729092
scholarrs794729092
googlers794729092
pharmgkbrs794729092
gwascentralrs794729092
openSNPrs794729092
23andMers794729092
23andMe allrs794729092
SNP Nexus

SNPshotrs794729092
SNPdbers794729092
MSV3drs794729092
GWAS Ctlgrs794729092
Max Magnitude0
ClinVar
Risk rs794729092(;)
Alt rs794729092(;)
Reference rs794729092(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene NEXN
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.78401701_78401702delAA
CLNSRC
CLNACC RCV000183680.2,