rs62641225

Orientation

minus

Stabilized

minus

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

Make rs62641225(G;T)

Make rs62641225(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2406561

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs62641225
dbSNP (classic)	rs62641225
ClinGen	rs62641225
ebi	rs62641225
HLI	rs62641225
Exac	rs62641225
Gnomad	rs62641225
Varsome	rs62641225
LitVar	rs62641225
Map	rs62641225
PheGenI	rs62641225
Biobank	rs62641225
1000 genomes	rs62641225
hgdp	rs62641225
ensembl	rs62641225
geneview	rs62641225
scholar	rs62641225
google	rs62641225
pharmgkb	rs62641225
gwascentral	rs62641225
openSNP	rs62641225
23andMe	rs62641225
SNPshot	rs62641225
SNPdbe	rs62641225
MSV3d	rs62641225
GWAS Ctlg	rs62641225

Max Magnitude

0

[PMID 15542397] The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.

ClinVar
Risk	rs62641225(A;A) rs62641225(T;T)
Alt	rs62641225(A;A) rs62641225(T;T)
Reference	Rs62641225(G;G)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 6A
Variation	info
Gene	PEX10
CLNDBN	Peroxisome biogenesis disorder 6A
Reversed	1
HGVS	NC_000001.10:g.2338000C>A
CLNSRC
CLNACC	RCV000289565.1,