rs369965266

Orientation

plus

Stabilized

plus

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

Make rs369965266(A;A)

Make rs369965266(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

2408700

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs369965266
dbSNP (classic)	rs369965266
ClinGen	rs369965266
ebi	rs369965266
HLI	rs369965266
Exac	rs369965266
Gnomad	rs369965266
Varsome	rs369965266
LitVar	rs369965266
Map	rs369965266
PheGenI	rs369965266
Biobank	rs369965266
1000 genomes	rs369965266
hgdp	rs369965266
ensembl	rs369965266
geneview	rs369965266
scholar	rs369965266
google	rs369965266
pharmgkb	rs369965266
gwascentral	rs369965266
openSNP	rs369965266
23andMe	rs369965266
SNPshot	rs369965266
SNPdbe	rs369965266
MSV3d	rs369965266
GWAS Ctlg	rs369965266

Max Magnitude

0

ClinVar
Risk	rs369965266(A;A)
Alt	rs369965266(A;A)
Reference	Rs369965266(G;G)
Significance	Probable-Pathogenic
Disease	Peroxisome biogenesis disorder 6A Peroxisome biogenesis disorder 6B
Variation	info
Gene	PEX10
CLNDBN	Peroxisome biogenesis disorder 6A Peroxisome biogenesis disorder 6B
Reversed	0
HGVS	NC_000001.10:g.2340139G>A
CLNSRC
CLNACC	RCV000410037.1, RCV000411504.1,