rs765661521

Orientation

plus

Stabilized

plus

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

Make rs765661521(A;A)

Make rs765661521(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

227303110

Gene	COL4A3, LOC654841

is a	snp
is	mentioned by
dbSNP	rs765661521
dbSNP (classic)	rs765661521
ClinGen	rs765661521
ebi	rs765661521
HLI	rs765661521
Exac	rs765661521
Gnomad	rs765661521
Varsome	rs765661521
LitVar	rs765661521
Map	rs765661521
PheGenI	rs765661521
Biobank	rs765661521
1000 genomes	rs765661521
hgdp	rs765661521
ensembl	rs765661521
geneview	rs765661521
scholar	rs765661521
google	rs765661521
pharmgkb	rs765661521
gwascentral	rs765661521
openSNP	rs765661521
23andMe	rs765661521
SNPshot	rs765661521
SNPdbe	rs765661521
MSV3d	rs765661521
GWAS Ctlg	rs765661521

Max Magnitude

0

ClinVar
Risk	rs765661521(A;A) rs765661521(C;C)
Alt	rs765661521(A;A) rs765661521(C;C)
Reference	Rs765661521(G;G)
Significance	Pathogenic
Disease	Alport syndrome
Variation	info
Gene	COL4A3 LOC654841
CLNDBN	Alport syndrome, autosomal recessive
Reversed	0
HGVS	NC_000002.11:g.228167826G>A
CLNSRC
CLNACC	RCV000415440.1,