rs267608190

Orientation

plus

Stabilized

plus

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

Make rs267608190(G;T)

Make rs267608190(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

18078607

Gene

PEX26

is a	snp
is	mentioned by
dbSNP	rs267608190
dbSNP (classic)	rs267608190
ClinGen	rs267608190
ebi	rs267608190
HLI	rs267608190
Exac	rs267608190
Gnomad	rs267608190
Varsome	rs267608190
LitVar	rs267608190
Map	rs267608190
PheGenI	rs267608190
Biobank	rs267608190
1000 genomes	rs267608190
hgdp	rs267608190
ensembl	rs267608190
geneview	rs267608190
scholar	rs267608190
google	rs267608190
pharmgkb	rs267608190
gwascentral	rs267608190
openSNP	rs267608190
23andMe	rs267608190
SNPshot	rs267608190
SNPdbe	rs267608190
MSV3d	rs267608190
GWAS Ctlg	rs267608190

Max Magnitude

0

ClinVar
Risk	rs267608190(T;T)
Alt	rs267608190(T;T)
Reference	Rs267608190(G;G)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 7A
Variation	info
Gene	PEX26
CLNDBN	Peroxisome biogenesis disorder 7A
Reversed	0
HGVS	NC_000022.10:g.18561373G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002242.2,