rs267606877

Orientation

plus

Stabilized

plus

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

Make rs267606877(C;C)

Make rs267606877(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

104703343

Gene

INF2

is a	snp
is	mentioned by
dbSNP	rs267606877
dbSNP (classic)	rs267606877
ClinGen	rs267606877
ebi	rs267606877
HLI	rs267606877
Exac	rs267606877
Gnomad	rs267606877
Varsome	rs267606877
LitVar	rs267606877
Map	rs267606877
PheGenI	rs267606877
Biobank	rs267606877
1000 genomes	rs267606877
hgdp	rs267606877
ensembl	rs267606877
geneview	rs267606877
scholar	rs267606877
google	rs267606877
pharmgkb	rs267606877
gwascentral	rs267606877
openSNP	rs267606877
23andMe	rs267606877
SNPshot	rs267606877
SNPdbe	rs267606877
MSV3d	rs267606877
GWAS Ctlg	rs267606877

Max Magnitude

0

ClinVar
Risk	rs267606877(C;C)
Alt	rs267606877(C;C)
Reference	Rs267606877(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.105169680T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001105.2,