rs139598219

Orientation

plus

Stabilized

plus

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

Make rs139598219(C;T)

Make rs139598219(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

35850407

Gene	KIRREL2, NPHS1

is a	snp
is	mentioned by
dbSNP	rs139598219
dbSNP (classic)	rs139598219
ClinGen	rs139598219
ebi	rs139598219
HLI	rs139598219
Exac	rs139598219
Gnomad	rs139598219
Varsome	rs139598219
LitVar	rs139598219
Map	rs139598219
PheGenI	rs139598219
Biobank	rs139598219
1000 genomes	rs139598219
hgdp	rs139598219
ensembl	rs139598219
geneview	rs139598219
scholar	rs139598219
google	rs139598219
pharmgkb	rs139598219
gwascentral	rs139598219
openSNP	rs139598219
23andMe	rs139598219
SNPshot	rs139598219
SNPdbe	rs139598219
MSV3d	rs139598219
GWAS Ctlg	rs139598219

Max Magnitude

0

ClinVar
Risk	rs139598219(A;A) rs139598219(T;T)
Alt	rs139598219(A;A) rs139598219(T;T)
Reference	Rs139598219(C;C)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1 KIRREL2
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	0
HGVS	NC_000019.9:g.36341309C>A
CLNSRC
CLNACC	RCV000169154.1,