rs1057517522

Orientation

minus

Stabilized

minus

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

Make rs1057517522(-;-)

Make rs1057517522(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

92517781

Gene

PEX1

is a	snp
is	mentioned by
dbSNP	rs1057517522
dbSNP (classic)	rs1057517522
ClinGen	rs1057517522
ebi	rs1057517522
HLI	rs1057517522
Exac	rs1057517522
Gnomad	rs1057517522
Varsome	rs1057517522
LitVar	rs1057517522
Map	rs1057517522
PheGenI	rs1057517522
Biobank	rs1057517522
1000 genomes	rs1057517522
hgdp	rs1057517522
ensembl	rs1057517522
geneview	rs1057517522
scholar	rs1057517522
google	rs1057517522
pharmgkb	rs1057517522
gwascentral	rs1057517522
openSNP	rs1057517522
23andMe	rs1057517522
SNPshot	rs1057517522
SNPdbe	rs1057517522
MSV3d	rs1057517522
GWAS Ctlg	rs1057517522

Max Magnitude

0

ClinVar
Risk	rs1057517522(-;-)
Alt	rs1057517522(-;-)
Reference	Rs1057517522(T;T)
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.92147095delA
CLNSRC
CLNACC	RCV000410891.1, RCV000411994.1,