rs376879175

Orientation

plus

Stabilized

plus

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

Make rs376879175(C;T)

Make rs376879175(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

100293039

Gene

INVS

is a	snp
is	mentioned by
dbSNP	rs376879175
dbSNP (classic)	rs376879175
ClinGen	rs376879175
ebi	rs376879175
HLI	rs376879175
Exac	rs376879175
Gnomad	rs376879175
Varsome	rs376879175
LitVar	rs376879175
Map	rs376879175
PheGenI	rs376879175
Biobank	rs376879175
1000 genomes	rs376879175
hgdp	rs376879175
ensembl	rs376879175
geneview	rs376879175
scholar	rs376879175
google	rs376879175
pharmgkb	rs376879175
gwascentral	rs376879175
openSNP	rs376879175
23andMe	rs376879175
SNPshot	rs376879175
SNPdbe	rs376879175
MSV3d	rs376879175
GWAS Ctlg	rs376879175

Max Magnitude

0

ClinVar
Risk	rs376879175(A;A) rs376879175(T;T)
Alt	rs376879175(A;A) rs376879175(T;T)
Reference	Rs376879175(C;C)
Significance	Other
Disease	Nephronophthisis
Variation	info
Gene	INVS
CLNDBN	Nephronophthisis
Reversed	0
HGVS	NC_000009.11:g.103055321C>T
CLNSRC
CLNACC	RCV000234833.2,