rs1057516662

Orientation

minus

Stabilized

minus

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

Make rs1057516662(-;-)

Make rs1057516662(-;GAGTGT)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

120652590

Gene

HGD

is a	snp
is	mentioned by
dbSNP	rs1057516662
dbSNP (classic)	rs1057516662
ClinGen	rs1057516662
ebi	rs1057516662
HLI	rs1057516662
Exac	rs1057516662
Gnomad	rs1057516662
Varsome	rs1057516662
LitVar	rs1057516662
Map	rs1057516662
PheGenI	rs1057516662
Biobank	rs1057516662
1000 genomes	rs1057516662
hgdp	rs1057516662
ensembl	rs1057516662
geneview	rs1057516662
scholar	rs1057516662
google	rs1057516662
pharmgkb	rs1057516662
gwascentral	rs1057516662
openSNP	rs1057516662
23andMe	rs1057516662
SNPshot	rs1057516662
SNPdbe	rs1057516662
MSV3d	rs1057516662
GWAS Ctlg	rs1057516662

Max Magnitude

0

ClinVar
Risk	rs1057516662(-;-)
Alt	rs1057516662(-;-)
Reference	Rs1057516662(GAGTGT;GAGTGT)
Significance	Probable-Pathogenic
Disease	Alkaptonuria
Variation	info
Gene	HGD
CLNDBN	Alkaptonuria
Reversed	1
HGVS	NC_000003.11:g.120371437_120371442delACACTC
CLNSRC
CLNACC	RCV000412288.1,