rs724160000

Orientation

minus

Stabilized

minus

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

Make rs724160000(C;C)

Make rs724160000(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

2406566

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs724160000
dbSNP (classic)	rs724160000
ClinGen	rs724160000
ebi	rs724160000
HLI	rs724160000
Exac	rs724160000
Gnomad	rs724160000
Varsome	rs724160000
LitVar	rs724160000
Map	rs724160000
PheGenI	rs724160000
Biobank	rs724160000
1000 genomes	rs724160000
hgdp	rs724160000
ensembl	rs724160000
geneview	rs724160000
scholar	rs724160000
google	rs724160000
pharmgkb	rs724160000
gwascentral	rs724160000
openSNP	rs724160000
23andMe	rs724160000
SNPshot	rs724160000
SNPdbe	rs724160000
MSV3d	rs724160000
GWAS Ctlg	rs724160000

Max Magnitude

0

ClinVar
Risk	rs724160000(C;C)
Alt	rs724160000(C;C)
Reference	Rs724160000(T;T)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 6B
Variation	info
Gene	PEX10
CLNDBN	Peroxisome biogenesis disorder 6B
Reversed	1
HGVS	NC_000001.10:g.2338005A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149810.4,