rs62636524

Orientation

minus

Stabilized

minus

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

Make rs62636524(-;-)

Make rs62636524(-;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2412499

Gene	PEX10, PLCH2

is a	snp
is	mentioned by
dbSNP	rs62636524
dbSNP (classic)	rs62636524
ClinGen	rs62636524
ebi	rs62636524
HLI	rs62636524
Exac	rs62636524
Gnomad	rs62636524
Varsome	rs62636524
LitVar	rs62636524
Map	rs62636524
PheGenI	rs62636524
Biobank	rs62636524
1000 genomes	rs62636524
hgdp	rs62636524
ensembl	rs62636524
geneview	rs62636524
scholar	rs62636524
google	rs62636524
pharmgkb	rs62636524
gwascentral	rs62636524
openSNP	rs62636524
23andMe	rs62636524
SNPshot	rs62636524
SNPdbe	rs62636524
MSV3d	rs62636524
GWAS Ctlg	rs62636524

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs62636524(G;G)
Significance	Untested
Disease
Variation	info
Gene	PEX10
CLNDBN
Reversed	1
HGVS	NC_000001.10:g.2343938delC
CLNSRC
CLNACC

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