rs267606878

Orientation

plus

Stabilized

plus

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

Make rs267606878(C;T)

Make rs267606878(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

104703439

Gene

INF2

is a	snp
is	mentioned by
dbSNP	rs267606878
dbSNP (classic)	rs267606878
ClinGen	rs267606878
ebi	rs267606878
HLI	rs267606878
Exac	rs267606878
Gnomad	rs267606878
Varsome	rs267606878
LitVar	rs267606878
Map	rs267606878
PheGenI	rs267606878
Biobank	rs267606878
1000 genomes	rs267606878
hgdp	rs267606878
ensembl	rs267606878
geneview	rs267606878
scholar	rs267606878
google	rs267606878
pharmgkb	rs267606878
gwascentral	rs267606878
openSNP	rs267606878
23andMe	rs267606878
SNPshot	rs267606878
SNPdbe	rs267606878
MSV3d	rs267606878
GWAS Ctlg	rs267606878

Max Magnitude

0

ClinVar
Risk	rs267606878(T;T)
Alt	rs267606878(T;T)
Reference	Rs267606878(C;C)
Significance	Pathogenic
Disease	Focal segmental glomerulosclerosis 5
Variation	info
Gene	INF2
CLNDBN	Focal segmental glomerulosclerosis 5
Reversed	0
HGVS	NC_000014.8:g.105169776C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001107.2,