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rs757674160

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs757674160(A;G)
Make rs757674160(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position56836704
GeneNUP93
is asnp
is mentioned by
dbSNPrs757674160
ebirs757674160
HLIrs757674160
Exacrs757674160
Varsomers757674160
Maprs757674160
PheGenIrs757674160
hapmaprs757674160
1000 genomesrs757674160
hgdprs757674160
ensemblrs757674160
gopubmedrs757674160
geneviewrs757674160
scholarrs757674160
googlers757674160
pharmgkbrs757674160
gwascentralrs757674160
openSNPrs757674160
23andMers757674160
23andMe allrs757674160
SNP Nexus

SNPshotrs757674160
SNPdbers757674160
MSV3drs757674160
GWAS Ctlgrs757674160
Max Magnitude0
ClinVar
Risk rs757674160(G;G)
Alt rs757674160(G;G)
Reference rs757674160(A;A)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NUP93
CLNDBN Nephrotic syndrome, type 12
Reversed 0
HGVS NC_000016.9:g.56870616A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210657.1,