rs757674160

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs757674160(A;G)

Make rs757674160(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

56836704

Gene

NUP93

is a	snp
is	mentioned by
dbSNP	rs757674160
dbSNP (classic)	rs757674160
ClinGen	rs757674160
ebi	rs757674160
HLI	rs757674160
Exac	rs757674160
Gnomad	rs757674160
Varsome	rs757674160
LitVar	rs757674160
Map	rs757674160
PheGenI	rs757674160
Biobank	rs757674160
1000 genomes	rs757674160
hgdp	rs757674160
ensembl	rs757674160
geneview	rs757674160
scholar	rs757674160
google	rs757674160
pharmgkb	rs757674160
gwascentral	rs757674160
openSNP	rs757674160
23andMe	rs757674160
SNPshot	rs757674160
SNPdbe	rs757674160
MSV3d	rs757674160
GWAS Ctlg	rs757674160

Max Magnitude

0

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,