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rs794729088

From SNPedia

Orientationplus
Geno Mag Summary
(AAAC;AAAC) 0 common in clinvar
Make rs794729088(-;-)
Make rs794729088(-;ACAA)
Make rs794729088(ACAA;ACAA)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position77925201
GeneNEXN
is asnp
is mentioned by
dbSNPrs794729088
ebirs794729088
HLIrs794729088
Exacrs794729088
Varsomers794729088
Maprs794729088
PheGenIrs794729088
hapmaprs794729088
1000 genomesrs794729088
hgdprs794729088
ensemblrs794729088
gopubmedrs794729088
geneviewrs794729088
scholarrs794729088
googlers794729088
pharmgkbrs794729088
gwascentralrs794729088
openSNPrs794729088
23andMers794729088
23andMe allrs794729088
SNP Nexus

SNPshotrs794729088
SNPdbers794729088
MSV3drs794729088
GWAS Ctlgrs794729088
Max Magnitude0
ClinVar
Risk rs794729088(;)
Alt rs794729088(;)
Reference rs794729088(AAAC;AAAC)
Significance Pathogenic
Disease not provided
Variation info
Gene NEXN
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.78390886_78390889delACAA
CLNSRC
CLNACC RCV000183676.2,