rs138909849

Orientation

plus

Stabilized

plus

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

Make rs138909849(A;A)

Make rs138909849(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

56833407

Gene

NUP93

is a	snp
is	mentioned by
dbSNP	rs138909849
dbSNP (classic)	rs138909849
ClinGen	rs138909849
ebi	rs138909849
HLI	rs138909849
Exac	rs138909849
Gnomad	rs138909849
Varsome	rs138909849
LitVar	rs138909849
Map	rs138909849
PheGenI	rs138909849
Biobank	rs138909849
1000 genomes	rs138909849
hgdp	rs138909849
ensembl	rs138909849
geneview	rs138909849
scholar	rs138909849
google	rs138909849
pharmgkb	rs138909849
gwascentral	rs138909849
openSNP	rs138909849
23andMe	rs138909849
SNPshot	rs138909849
SNPdbe	rs138909849
MSV3d	rs138909849
GWAS Ctlg	rs138909849

Max Magnitude

0

ClinVar
Risk	rs138909849(A;A)
Alt	rs138909849(A;A)
Reference	Rs138909849(G;G)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	NUP93
CLNDBN	Nephrotic syndrome, type 12
Reversed	0
HGVS	NC_000016.9:g.56867319G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210572.1,