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rs864321632

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321632(A;C)
Make rs864321632(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position68735334
GeneNUP107
is asnp
is mentioned by
dbSNPrs864321632
ebirs864321632
HLIrs864321632
Exacrs864321632
Varsomers864321632
Maprs864321632
PheGenIrs864321632
hapmaprs864321632
1000 genomesrs864321632
hgdprs864321632
ensemblrs864321632
gopubmedrs864321632
geneviewrs864321632
scholarrs864321632
googlers864321632
pharmgkbrs864321632
gwascentralrs864321632
openSNPrs864321632
23andMers864321632
23andMe allrs864321632
SNP Nexus

SNPshotrs864321632
SNPdbers864321632
MSV3drs864321632
GWAS Ctlgrs864321632
Max Magnitude0
ClinVar
Risk rs864321632(C;C)
Alt rs864321632(C;C)
Reference rs864321632(A;A)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NUP107
CLNDBN Nephrotic syndrome, type 11
Reversed 0
HGVS NC_000012.11:g.69129114A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000203507.1,