rs267607183

Orientation

plus

Stabilized

plus

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

Make rs267607183(A;A)

Make rs267607183(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

104703440

Gene

INF2

is a	snp
is	mentioned by
dbSNP	rs267607183
dbSNP (classic)	rs267607183
ClinGen	rs267607183
ebi	rs267607183
HLI	rs267607183
Exac	rs267607183
Gnomad	rs267607183
Varsome	rs267607183
LitVar	rs267607183
Map	rs267607183
PheGenI	rs267607183
Biobank	rs267607183
1000 genomes	rs267607183
hgdp	rs267607183
ensembl	rs267607183
geneview	rs267607183
scholar	rs267607183
google	rs267607183
pharmgkb	rs267607183
gwascentral	rs267607183
openSNP	rs267607183
23andMe	rs267607183
SNPshot	rs267607183
SNPdbe	rs267607183
MSV3d	rs267607183
GWAS Ctlg	rs267607183

Max Magnitude

0

ClinVar
Risk	rs267607183(A;A)
Alt	rs267607183(A;A)
Reference	Rs267607183(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.105169777G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001106.2,