rs267606879

Orientation

plus

Stabilized

plus

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

Make rs267606879(A;A)

Make rs267606879(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

104703428

Gene

INF2

is a	snp
is	mentioned by
dbSNP	rs267606879
dbSNP (classic)	rs267606879
ClinGen	rs267606879
ebi	rs267606879
HLI	rs267606879
Exac	rs267606879
Gnomad	rs267606879
Varsome	rs267606879
LitVar	rs267606879
Map	rs267606879
PheGenI	rs267606879
Biobank	rs267606879
1000 genomes	rs267606879
hgdp	rs267606879
ensembl	rs267606879
geneview	rs267606879
scholar	rs267606879
google	rs267606879
pharmgkb	rs267606879
gwascentral	rs267606879
openSNP	rs267606879
23andMe	rs267606879
SNPshot	rs267606879
SNPdbe	rs267606879
MSV3d	rs267606879
GWAS Ctlg	rs267606879

Max Magnitude

0

ClinVar
Risk	rs267606879(A;A)
Alt	rs267606879(A;A)
Reference	Rs267606879(G;G)
Significance	Pathogenic
Disease	Focal segmental glomerulosclerosis 5
Variation	info
Gene	INF2
CLNDBN	Focal segmental glomerulosclerosis 5
Reversed	0
HGVS	NC_000014.8:g.105169765G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001108.2,