rs150038620

Orientation

plus

Stabilized

plus

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

Make rs150038620(C;T)

Make rs150038620(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

35842551

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs150038620
dbSNP (classic)	rs150038620
ClinGen	rs150038620
ebi	rs150038620
HLI	rs150038620
Exac	rs150038620
Gnomad	rs150038620
Varsome	rs150038620
LitVar	rs150038620
Map	rs150038620
PheGenI	rs150038620
Biobank	rs150038620
1000 genomes	rs150038620
hgdp	rs150038620
ensembl	rs150038620
geneview	rs150038620
scholar	rs150038620
google	rs150038620
pharmgkb	rs150038620
gwascentral	rs150038620
openSNP	rs150038620
23andMe	rs150038620
SNPshot	rs150038620
SNPdbe	rs150038620
MSV3d	rs150038620
GWAS Ctlg	rs150038620

Max Magnitude

0

ClinVar
Risk	rs150038620(T;T)
Alt	rs150038620(T;T)
Reference	Rs150038620(C;C)
Significance	Other
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	0
HGVS	NC_000019.9:g.36333453C>T
CLNSRC
CLNACC	RCV000169038.1,