rs797044762

Orientation

minus

Stabilized

minus

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

Make rs797044762(-;G)

Make rs797044762(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

2406528

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs797044762
dbSNP (classic)	rs797044762
ClinGen	rs797044762
ebi	rs797044762
HLI	rs797044762
Exac	rs797044762
Gnomad	rs797044762
Varsome	rs797044762
LitVar	rs797044762
Map	rs797044762
PheGenI	rs797044762
Biobank	rs797044762
1000 genomes	rs797044762
hgdp	rs797044762
ensembl	rs797044762
geneview	rs797044762
scholar	rs797044762
google	rs797044762
pharmgkb	rs797044762
gwascentral	rs797044762
openSNP	rs797044762
23andMe	rs797044762
SNPshot	rs797044762
SNPdbe	rs797044762
MSV3d	rs797044762
GWAS Ctlg	rs797044762

Max Magnitude

0

ClinVar
Risk	rs797044762(G;G)
Alt	rs797044762(G;G)
Reference	Rs797044762(-;-)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 6A
Variation	info
Gene	PEX10
CLNDBN	Peroxisome biogenesis disorder 6A
Reversed	1
HGVS	NC_000001.10:g.2337967_2337968insC
CLNSRC
CLNACC	RCV000179026.1,