rs267608176

Orientation

minus

Stabilized

minus

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

Make rs267608176(-;-)

Make rs267608176(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

92506306

Gene

PEX1

is a	snp
is	mentioned by
dbSNP	rs267608176
dbSNP (classic)	rs267608176
ClinGen	rs267608176
ebi	rs267608176
HLI	rs267608176
Exac	rs267608176
Gnomad	rs267608176
Varsome	rs267608176
LitVar	rs267608176
Map	rs267608176
PheGenI	rs267608176
Biobank	rs267608176
1000 genomes	rs267608176
hgdp	rs267608176
ensembl	rs267608176
geneview	rs267608176
scholar	rs267608176
google	rs267608176
pharmgkb	rs267608176
gwascentral	rs267608176
openSNP	rs267608176
23andMe	rs267608176
SNPshot	rs267608176
SNPdbe	rs267608176
MSV3d	rs267608176
GWAS Ctlg	rs267608176

Max Magnitude

0

ClinVar
Risk	rs267608176(-;-)
Alt	rs267608176(-;-)
Reference	Rs267608176(A;A)
Significance	Probable-Pathogenic
Disease	Zellweger syndrome Peroxisome biogenesis disorder 1B
Variation	info
Gene	PEX1
CLNDBN	Zellweger syndrome Peroxisome biogenesis disorder 1B
Reversed	1
HGVS	NC_000007.13:g.92135620delT
CLNSRC
CLNACC	RCV000410765.1, RCV000412291.1,