rs878855333

Orientation

plus

Stabilized

plus

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

Make rs878855333(-;-)

Make rs878855333(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

100300601

Gene

INVS

is a	snp
is	mentioned by
dbSNP	rs878855333
dbSNP (classic)	rs878855333
ClinGen	rs878855333
ebi	rs878855333
HLI	rs878855333
Exac	rs878855333
Gnomad	rs878855333
Varsome	rs878855333
LitVar	rs878855333
Map	rs878855333
PheGenI	rs878855333
Biobank	rs878855333
1000 genomes	rs878855333
hgdp	rs878855333
ensembl	rs878855333
geneview	rs878855333
scholar	rs878855333
google	rs878855333
pharmgkb	rs878855333
gwascentral	rs878855333
openSNP	rs878855333
23andMe	rs878855333
SNPshot	rs878855333
SNPdbe	rs878855333
MSV3d	rs878855333
GWAS Ctlg	rs878855333

Max Magnitude

0

ClinVar
Risk	rs878855333(-;-)
Alt	rs878855333(-;-)
Reference	Rs878855333(A;A)
Significance	Pathogenic
Disease	Nephronophthisis
Variation	info
Gene	INVS
CLNDBN	Nephronophthisis
Reversed	0
HGVS	NC_000009.11:g.103062883delA
CLNSRC
CLNACC	RCV000234816.1,