rs61752094

Orientation

minus

Stabilized

minus

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

Make rs61752094(C;G)

Make rs61752094(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2406528

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs61752094
dbSNP (classic)	rs61752094
ClinGen	rs61752094
ebi	rs61752094
HLI	rs61752094
Exac	rs61752094
Gnomad	rs61752094
Varsome	rs61752094
LitVar	rs61752094
Map	rs61752094
PheGenI	rs61752094
Biobank	rs61752094
1000 genomes	rs61752094
hgdp	rs61752094
ensembl	rs61752094
geneview	rs61752094
scholar	rs61752094
google	rs61752094
pharmgkb	rs61752094
gwascentral	rs61752094
openSNP	rs61752094
23andMe	rs61752094
SNPshot	rs61752094
SNPdbe	rs61752094
MSV3d	rs61752094
GWAS Ctlg	rs61752094

Max Magnitude

0

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

ClinVar
Risk	rs61752094(G;G)
Alt	rs61752094(G;G)
Reference	Rs61752094(C;C)
Significance	Untested
Disease
Variation	info
Gene	PEX10
CLNDBN
Reversed	1
HGVS	NC_000001.10:g.2337967G>C
CLNSRC
CLNACC