rs587777741

Orientation

plus

Stabilized

plus

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

Make rs587777741(C;T)

Make rs587777741(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

36411062

Gene

ANLN

is a	snp
is	mentioned by
dbSNP	rs587777741
dbSNP (classic)	rs587777741
ClinGen	rs587777741
ebi	rs587777741
HLI	rs587777741
Exac	rs587777741
Gnomad	rs587777741
Varsome	rs587777741
LitVar	rs587777741
Map	rs587777741
PheGenI	rs587777741
Biobank	rs587777741
1000 genomes	rs587777741
hgdp	rs587777741
ensembl	rs587777741
geneview	rs587777741
scholar	rs587777741
google	rs587777741
pharmgkb	rs587777741
gwascentral	rs587777741
openSNP	rs587777741
23andMe	rs587777741
SNPshot	rs587777741
SNPdbe	rs587777741
MSV3d	rs587777741
GWAS Ctlg	rs587777741

Max Magnitude

0

ClinVar
Risk	rs587777741(T;T)
Alt	rs587777741(T;T)
Reference	Rs587777741(C;C)
Significance	Pathogenic
Disease	Focal segmental glomerulosclerosis 8
Variation	info
Gene	ANLN
CLNDBN	Focal segmental glomerulosclerosis 8
Reversed	0
HGVS	NC_000007.13:g.36450671C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000144242.5,