rs267606880

Orientation

plus

Stabilized

plus

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

Make rs267606880(C;C)

Make rs267606880(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

104701490

Gene

INF2

is a	snp
is	mentioned by
dbSNP	rs267606880
dbSNP (classic)	rs267606880
ClinGen	rs267606880
ebi	rs267606880
HLI	rs267606880
Exac	rs267606880
Gnomad	rs267606880
Varsome	rs267606880
LitVar	rs267606880
Map	rs267606880
PheGenI	rs267606880
Biobank	rs267606880
1000 genomes	rs267606880
hgdp	rs267606880
ensembl	rs267606880
geneview	rs267606880
scholar	rs267606880
google	rs267606880
pharmgkb	rs267606880
gwascentral	rs267606880
openSNP	rs267606880
23andMe	rs267606880
SNPshot	rs267606880
SNPdbe	rs267606880
MSV3d	rs267606880
GWAS Ctlg	rs267606880

Max Magnitude

0

ClinVar
Risk	rs267606880(C;C)
Alt	rs267606880(C;C)
Reference	Rs267606880(T;T)
Significance	Pathogenic
Disease	Focal segmental glomerulosclerosis 5
Variation	info
Gene	INF2
CLNDBN	Focal segmental glomerulosclerosis 5
Reversed	0
HGVS	NC_000014.8:g.105167827T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001109.2,