rs724159999

Orientation

minus

Stabilized

minus

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

Make rs724159999(-;-)

Make rs724159999(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

2408715

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs724159999
dbSNP (classic)	rs724159999
ClinGen	rs724159999
ebi	rs724159999
HLI	rs724159999
Exac	rs724159999
Gnomad	rs724159999
Varsome	rs724159999
LitVar	rs724159999
Map	rs724159999
PheGenI	rs724159999
Biobank	rs724159999
1000 genomes	rs724159999
hgdp	rs724159999
ensembl	rs724159999
geneview	rs724159999
scholar	rs724159999
google	rs724159999
pharmgkb	rs724159999
gwascentral	rs724159999
openSNP	rs724159999
23andMe	rs724159999
SNPshot	rs724159999
SNPdbe	rs724159999
MSV3d	rs724159999
GWAS Ctlg	rs724159999

Max Magnitude

0

ClinVar
Risk	rs724159999(-;-)
Alt	rs724159999(-;-)
Reference	Rs724159999(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.2340154delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149809.4,