rs369162678

Orientation

plus

Stabilized

plus

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

Make rs369162678(A;A)

Make rs369162678(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

5863955

Gene	NPHP4, MIR4689

is a	snp
is	mentioned by
dbSNP	rs369162678
dbSNP (classic)	rs369162678
ClinGen	rs369162678
ebi	rs369162678
HLI	rs369162678
Exac	rs369162678
Gnomad	rs369162678
Varsome	rs369162678
LitVar	rs369162678
Map	rs369162678
PheGenI	rs369162678
Biobank	rs369162678
1000 genomes	rs369162678
hgdp	rs369162678
ensembl	rs369162678
geneview	rs369162678
scholar	rs369162678
google	rs369162678
pharmgkb	rs369162678
gwascentral	rs369162678
openSNP	rs369162678
23andMe	rs369162678
SNPshot	rs369162678
SNPdbe	rs369162678
MSV3d	rs369162678
GWAS Ctlg	rs369162678

Max Magnitude

0

ClinVar
Risk	rs369162678(A;A)
Alt	rs369162678(A;A)
Reference	Rs369162678(G;G)
Significance	Probable-Pathogenic
Disease	not provided Renal dysplasia and retinal aplasia Nephronophthisis
Variation	info
Gene	NPHP4 MIR4689
CLNDBN	not provided Renal dysplasia and retinal aplasia Nephronophthisis
Reversed	0
HGVS	NC_000001.10:g.5924015G>A
CLNSRC	Illumina
CLNACC	RCV000171146.1, RCV000308383.1, RCV000346948.1,