rs61752096

Orientation

minus

Stabilized

minus

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

Make rs61752096(A;A)

Make rs61752096(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2406515

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs61752096
dbSNP (classic)	rs61752096
ClinGen	rs61752096
ebi	rs61752096
HLI	rs61752096
Exac	rs61752096
Gnomad	rs61752096
Varsome	rs61752096
LitVar	rs61752096
Map	rs61752096
PheGenI	rs61752096
Biobank	rs61752096
1000 genomes	rs61752096
hgdp	rs61752096
ensembl	rs61752096
geneview	rs61752096
scholar	rs61752096
google	rs61752096
pharmgkb	rs61752096
gwascentral	rs61752096
openSNP	rs61752096
23andMe	rs61752096
SNPshot	rs61752096
SNPdbe	rs61752096
MSV3d	rs61752096
GWAS Ctlg	rs61752096

Max Magnitude

0

[PMID 17041890] Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.

ClinVar
Risk	rs61752096(A;A)
Alt	rs61752096(A;A)
Reference	Rs61752096(G;G)
Significance	Untested
Disease
Variation	info
Gene	PEX10
CLNDBN
Reversed	1
HGVS	NC_000001.10:g.2337954C>T
CLNSRC
CLNACC