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rs864321688

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321688(A;A)
Make rs864321688(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position68713809
GeneNUP107
is asnp
is mentioned by
dbSNPrs864321688
ebirs864321688
HLIrs864321688
Exacrs864321688
Varsomers864321688
Maprs864321688
PheGenIrs864321688
hapmaprs864321688
1000 genomesrs864321688
hgdprs864321688
ensemblrs864321688
gopubmedrs864321688
geneviewrs864321688
scholarrs864321688
googlers864321688
pharmgkbrs864321688
gwascentralrs864321688
openSNPrs864321688
23andMers864321688
23andMe allrs864321688
SNP Nexus

SNPshotrs864321688
SNPdbers864321688
MSV3drs864321688
GWAS Ctlgrs864321688
Max Magnitude0
ClinVar
Risk rs864321688(A;A)
Alt rs864321688(A;A)
Reference rs864321688(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NUP107
CLNDBN Nephrotic syndrome, type 11
Reversed 0
HGVS NC_000012.11:g.69107589G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000203541.1,