rs1057524695

Orientation

minus

Stabilized

minus

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

Make rs1057524695(A;T)

Make rs1057524695(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35831049

Gene

NPHS1

is a	snp
is	mentioned by
dbSNP	rs1057524695
dbSNP (classic)	rs1057524695
ClinGen	rs1057524695
ebi	rs1057524695
HLI	rs1057524695
Exac	rs1057524695
Gnomad	rs1057524695
Varsome	rs1057524695
LitVar	rs1057524695
Map	rs1057524695
PheGenI	rs1057524695
Biobank	rs1057524695
1000 genomes	rs1057524695
hgdp	rs1057524695
ensembl	rs1057524695
geneview	rs1057524695
scholar	rs1057524695
google	rs1057524695
pharmgkb	rs1057524695
gwascentral	rs1057524695
openSNP	rs1057524695
23andMe	rs1057524695
SNPshot	rs1057524695
SNPdbe	rs1057524695
MSV3d	rs1057524695
GWAS Ctlg	rs1057524695

Max Magnitude

0

ClinVar
Risk	rs1057524695(T;T)
Alt	rs1057524695(T;T)
Reference	Rs1057524695(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NPHS1
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.36321951T>A
CLNSRC
CLNACC	RCV000442634.1,