rs149806989

Orientation

plus

Stabilized

plus

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

Make rs149806989(A;A)

Make rs149806989(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

92517968

Gene

PEX1

is a	snp
is	mentioned by
dbSNP	rs149806989
dbSNP (classic)	rs149806989
ClinGen	rs149806989
ebi	rs149806989
HLI	rs149806989
Exac	rs149806989
Gnomad	rs149806989
Varsome	rs149806989
LitVar	rs149806989
Map	rs149806989
PheGenI	rs149806989
Biobank	rs149806989
1000 genomes	rs149806989
hgdp	rs149806989
ensembl	rs149806989
geneview	rs149806989
scholar	rs149806989
google	rs149806989
pharmgkb	rs149806989
gwascentral	rs149806989
openSNP	rs149806989
23andMe	rs149806989
SNPshot	rs149806989
SNPdbe	rs149806989
MSV3d	rs149806989
GWAS Ctlg	rs149806989

Max Magnitude

0

ClinVar
Risk	rs149806989(A;A)
Alt	rs149806989(A;A)
Reference	Rs149806989(G;G)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 1B Zellweger syndrome
Variation	info
Gene	PEX1
CLNDBN	Peroxisome biogenesis disorder 1B Zellweger syndrome
Reversed	0
HGVS	NC_000007.13:g.92147282G>A
CLNSRC
CLNACC	RCV000409397.1, RCV000411910.1,