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rs397517858

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517858(A;G)
Make rs397517858(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position77918218
GeneNEXN
is asnp
is mentioned by
dbSNPrs397517858
ebirs397517858
HLIrs397517858
Exacrs397517858
Varsomers397517858
Maprs397517858
PheGenIrs397517858
hapmaprs397517858
1000 genomesrs397517858
hgdprs397517858
ensemblrs397517858
gopubmedrs397517858
geneviewrs397517858
scholarrs397517858
googlers397517858
pharmgkbrs397517858
gwascentralrs397517858
openSNPrs397517858
23andMers397517858
23andMe allrs397517858
SNP Nexus

SNPshotrs397517858
SNPdbers397517858
MSV3drs397517858
GWAS Ctlgrs397517858
Max Magnitude0
ClinVar
Risk rs397517858(G;G)
Alt rs397517858(G;G)
Reference rs397517858(A;A)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene NEXN
CLNDBN not specified Cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.78383903A>G
CLNSRC
CLNACC RCV000041178.2, RCV000183649.1,