rs61752092

Orientation

minus

Stabilized

minus

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

Make rs61752092(C;T)

Make rs61752092(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2406766

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs61752092
dbSNP (classic)	rs61752092
ClinGen	rs61752092
ebi	rs61752092
HLI	rs61752092
Exac	rs61752092
Gnomad	rs61752092
Varsome	rs61752092
LitVar	rs61752092
Map	rs61752092
PheGenI	rs61752092
Biobank	rs61752092
1000 genomes	rs61752092
hgdp	rs61752092
ensembl	rs61752092
geneview	rs61752092
scholar	rs61752092
google	rs61752092
pharmgkb	rs61752092
gwascentral	rs61752092
openSNP	rs61752092
23andMe	rs61752092
SNPshot	rs61752092
SNPdbe	rs61752092
MSV3d	rs61752092
GWAS Ctlg	rs61752092

Max Magnitude

0

ClinVar
Risk	rs61752092(G;G) rs61752092(T;T)
Alt	rs61752092(G;G) rs61752092(T;T)
Reference	Rs61752092(C;C)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 6B
Variation	info
Gene	PEX10
CLNDBN	Peroxisome biogenesis disorder 6B
Reversed	1
HGVS	NC_000001.10:g.2338205G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149813.4,

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