rs1057517499

Orientation

minus

Stabilized

minus

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

Make rs1057517499(-;-)

Make rs1057517499(-;TACTT)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

92503101

Gene

PEX1

is a	snp
is	mentioned by
dbSNP	rs1057517499
dbSNP (classic)	rs1057517499
ClinGen	rs1057517499
ebi	rs1057517499
HLI	rs1057517499
Exac	rs1057517499
Gnomad	rs1057517499
Varsome	rs1057517499
LitVar	rs1057517499
Map	rs1057517499
PheGenI	rs1057517499
Biobank	rs1057517499
1000 genomes	rs1057517499
hgdp	rs1057517499
ensembl	rs1057517499
geneview	rs1057517499
scholar	rs1057517499
google	rs1057517499
pharmgkb	rs1057517499
gwascentral	rs1057517499
openSNP	rs1057517499
23andMe	rs1057517499
SNPshot	rs1057517499
SNPdbe	rs1057517499
MSV3d	rs1057517499
GWAS Ctlg	rs1057517499

Max Magnitude

0

ClinVar
Risk	rs1057517499(-;-)
Alt	rs1057517499(-;-)
Reference	Rs1057517499(TACTT;TACTT)
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.92132415_92132419delAAGTA
CLNSRC
CLNACC	RCV000410634.1, RCV000411755.1,