rs267608183

Orientation

minus

Stabilized

minus

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

Make rs267608183(A;A)

Make rs267608183(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

2408451

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs267608183
dbSNP (classic)	rs267608183
ClinGen	rs267608183
ebi	rs267608183
HLI	rs267608183
Exac	rs267608183
Gnomad	rs267608183
Varsome	rs267608183
LitVar	rs267608183
Map	rs267608183
PheGenI	rs267608183
Biobank	rs267608183
1000 genomes	rs267608183
hgdp	rs267608183
ensembl	rs267608183
geneview	rs267608183
scholar	rs267608183
google	rs267608183
pharmgkb	rs267608183
gwascentral	rs267608183
openSNP	rs267608183
23andMe	rs267608183
SNPshot	rs267608183
SNPdbe	rs267608183
MSV3d	rs267608183
GWAS Ctlg	rs267608183

Max Magnitude

0

ClinVar
Risk	rs267608183(A;A)
Alt	rs267608183(A;A)
Reference	Rs267608183(G;G)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 6A
Variation	info
Gene	PEX10
CLNDBN	Peroxisome biogenesis disorder 6A
Reversed	1
HGVS	NC_000001.10:g.2339890C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007172.3,