rs61752122

Orientation

minus

Stabilized

minus

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

Make rs61752122(-;-)

Make rs61752122(-;GAGAT)

Reference

GRCh38 38.1/142

Chromosome

8

Position

76983896

Gene

PEX2

is a	snp
is	mentioned by
dbSNP	rs61752122
dbSNP (classic)	rs61752122
ClinGen	rs61752122
ebi	rs61752122
HLI	rs61752122
Exac	rs61752122
Gnomad	rs61752122
Varsome	rs61752122
LitVar	rs61752122
Map	rs61752122
PheGenI	rs61752122
Biobank	rs61752122
1000 genomes	rs61752122
hgdp	rs61752122
ensembl	rs61752122
geneview	rs61752122
scholar	rs61752122
google	rs61752122
pharmgkb	rs61752122
gwascentral	rs61752122
openSNP	rs61752122
23andMe	rs61752122
SNPshot	rs61752122
SNPdbe	rs61752122
MSV3d	rs61752122
GWAS Ctlg	rs61752122

Max Magnitude

0

ClinVar
Risk	rs61752122(-;-)
Alt	rs61752122(-;-)
Reference	Rs61752122(GAGAT;GAGAT)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 5a (zellweger)
Variation	info
Gene	PEX2
CLNDBN	Peroxisome biogenesis disorder 5a (zellweger)
Reversed	1
HGVS	NC_000008.10:g.77896132_77896136delATCTC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128529.3,