rs61752093

Orientation

minus

Stabilized

minus

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

Make rs61752093(-;-)

Make rs61752093(-;CT)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

2406581

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs61752093
dbSNP (classic)	rs61752093
ClinGen	rs61752093
ebi	rs61752093
HLI	rs61752093
Exac	rs61752093
Gnomad	rs61752093
Varsome	rs61752093
LitVar	rs61752093
Map	rs61752093
PheGenI	rs61752093
Biobank	rs61752093
1000 genomes	rs61752093
hgdp	rs61752093
ensembl	rs61752093
geneview	rs61752093
scholar	rs61752093
google	rs61752093
pharmgkb	rs61752093
gwascentral	rs61752093
openSNP	rs61752093
23andMe	rs61752093
SNPshot	rs61752093
SNPdbe	rs61752093
MSV3d	rs61752093
GWAS Ctlg	rs61752093

Max Magnitude

0

ClinVar
Risk	rs61752093(-;-)
Alt	rs61752093(-;-)
Reference	Rs61752093(CT;CT)
Significance	Pathogenic
Disease	Zellweger syndrome Peroxisome biogenesis disorder 6B Peroxisome biogenesis disorder 6A
Variation	info
Gene	PEX10
CLNDBN	Zellweger syndrome Peroxisome biogenesis disorder 6B Peroxisome biogenesis disorder 6A
Reversed	1
HGVS	NC_000001.10:g.2338020_2338021delAG
CLNSRC	Illumina
CLNACC	RCV000337969.1, RCV000409050.1, RCV000411962.1,