rs778217926

Orientation

plus

Stabilized

plus

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

Make rs778217926(-;-)

Make rs778217926(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35849643

Gene	KIRREL2, NPHS1

is a	snp
is	mentioned by
dbSNP	rs778217926
dbSNP (classic)	rs778217926
ClinGen	rs778217926
ebi	rs778217926
HLI	rs778217926
Exac	rs778217926
Gnomad	rs778217926
Varsome	rs778217926
LitVar	rs778217926
Map	rs778217926
PheGenI	rs778217926
Biobank	rs778217926
1000 genomes	rs778217926
hgdp	rs778217926
ensembl	rs778217926
geneview	rs778217926
scholar	rs778217926
google	rs778217926
pharmgkb	rs778217926
gwascentral	rs778217926
openSNP	rs778217926
23andMe	rs778217926
SNPshot	rs778217926
SNPdbe	rs778217926
MSV3d	rs778217926
GWAS Ctlg	rs778217926

Max Magnitude

0

ClinVar
Risk	rs778217926(-;-)
Alt	rs778217926(-;-)
Reference	Rs778217926(G;G)
Significance	Probable-Pathogenic
Disease	Finnish congenital nephrotic syndrome
Variation	info
Gene	NPHS1
CLNDBN	Finnish congenital nephrotic syndrome
Reversed	0
HGVS	NC_000019.9:g.36340545delG
CLNSRC
CLNACC	RCV000412108.1,