rs878855332

Orientation

plus

Stabilized

plus

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

Make rs878855332(-;-)

Make rs878855332(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

100253089

Gene

INVS

is a	snp
is	mentioned by
dbSNP	rs878855332
dbSNP (classic)	rs878855332
ClinGen	rs878855332
ebi	rs878855332
HLI	rs878855332
Exac	rs878855332
Gnomad	rs878855332
Varsome	rs878855332
LitVar	rs878855332
Map	rs878855332
PheGenI	rs878855332
Biobank	rs878855332
1000 genomes	rs878855332
hgdp	rs878855332
ensembl	rs878855332
geneview	rs878855332
scholar	rs878855332
google	rs878855332
pharmgkb	rs878855332
gwascentral	rs878855332
openSNP	rs878855332
23andMe	rs878855332
SNPshot	rs878855332
SNPdbe	rs878855332
MSV3d	rs878855332
GWAS Ctlg	rs878855332

Max Magnitude

0

ClinVar
Risk	rs878855332(-;-)
Alt	rs878855332(-;-)
Reference	Rs878855332(G;G)
Significance	Pathogenic
Disease	Nephronophthisis
Variation	info
Gene	INVS
CLNDBN	Nephronophthisis
Reversed	0
HGVS	NC_000009.11:g.103015371delG
CLNSRC
CLNACC	RCV000234834.1,