rs2491097

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common on affy axiom data

Make rs2491097(C;T)

Make rs2491097(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

100240169

Gene

INVS

is a	snp
is	mentioned by
dbSNP	rs2491097
dbSNP (classic)	rs2491097
ClinGen	rs2491097
ebi	rs2491097
HLI	rs2491097
Exac	rs2491097
Gnomad	rs2491097
Varsome	rs2491097
LitVar	rs2491097
Map	rs2491097
PheGenI	rs2491097
Biobank	rs2491097
1000 genomes	rs2491097
hgdp	rs2491097
ensembl	rs2491097
geneview	rs2491097
scholar	rs2491097
google	rs2491097
pharmgkb	rs2491097
gwascentral	rs2491097
openSNP	rs2491097
23andMe	rs2491097
SNPshot	rs2491097
SNPdbe	rs2491097
MSV3d	rs2491097
GWAS Ctlg	rs2491097

GMAF

0.004591

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs2491097(T;T)
Alt	rs2491097(T;T)
Reference	Rs2491097(C;C)
Significance	Non-pathogenic
Disease	not specified Nephronophthisis
Variation	info
Gene	INVS
CLNDBN	not specified Nephronophthisis
Reversed	0
HGVS	NC_000009.11:g.103002451C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000081631.5, RCV000473554.1,