rs1057523689

Orientation

plus

Stabilized

plus

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

Make rs1057523689(A;A)

Make rs1057523689(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

143485201

Gene

PEX3

is a	snp
is	mentioned by
dbSNP	rs1057523689
dbSNP (classic)	rs1057523689
ClinGen	rs1057523689
ebi	rs1057523689
HLI	rs1057523689
Exac	rs1057523689
Gnomad	rs1057523689
Varsome	rs1057523689
LitVar	rs1057523689
Map	rs1057523689
PheGenI	rs1057523689
Biobank	rs1057523689
1000 genomes	rs1057523689
hgdp	rs1057523689
ensembl	rs1057523689
geneview	rs1057523689
scholar	rs1057523689
google	rs1057523689
pharmgkb	rs1057523689
gwascentral	rs1057523689
openSNP	rs1057523689
23andMe	rs1057523689
SNPshot	rs1057523689
SNPdbe	rs1057523689
MSV3d	rs1057523689
GWAS Ctlg	rs1057523689

Max Magnitude

0

ClinVar
Risk	rs1057523689(A;A)
Alt	rs1057523689(A;A)
Reference	Rs1057523689(G;G)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 10b
Variation	info
Gene	PEX3
CLNDBN	Peroxisome biogenesis disorder 10b
Reversed	0
HGVS	NC_000006.11:g.143806338G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000433323.1,