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rs864321633

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321633(G;T)
Make rs864321633(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position68696839
GeneNUP107
is asnp
is mentioned by
dbSNPrs864321633
ebirs864321633
HLIrs864321633
Exacrs864321633
Varsomers864321633
Maprs864321633
PheGenIrs864321633
hapmaprs864321633
1000 genomesrs864321633
hgdprs864321633
ensemblrs864321633
gopubmedrs864321633
geneviewrs864321633
scholarrs864321633
googlers864321633
pharmgkbrs864321633
gwascentralrs864321633
openSNPrs864321633
23andMers864321633
23andMe allrs864321633
SNP Nexus

SNPshotrs864321633
SNPdbers864321633
MSV3drs864321633
GWAS Ctlgrs864321633
Max Magnitude0
ClinVar
Risk rs864321633(T;T)
Alt rs864321633(T;T)
Reference rs864321633(G;G)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NUP107
CLNDBN Nephrotic syndrome, type 11
Reversed 0
HGVS NC_000012.11:g.69090619G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203505.1,