rs61752129

Orientation

plus

Stabilized

plus

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

Make rs61752129(-;C)

Make rs61752129(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

22

Position

18078410

Gene

PEX26

is a	snp
is	mentioned by
dbSNP	rs61752129
dbSNP (classic)	rs61752129
ClinGen	rs61752129
ebi	rs61752129
HLI	rs61752129
Exac	rs61752129
Gnomad	rs61752129
Varsome	rs61752129
LitVar	rs61752129
Map	rs61752129
PheGenI	rs61752129
Biobank	rs61752129
1000 genomes	rs61752129
hgdp	rs61752129
ensembl	rs61752129
geneview	rs61752129
scholar	rs61752129
google	rs61752129
pharmgkb	rs61752129
gwascentral	rs61752129
openSNP	rs61752129
23andMe	rs61752129
SNPshot	rs61752129
SNPdbe	rs61752129
MSV3d	rs61752129
GWAS Ctlg	rs61752129

Max Magnitude

0

ClinVar
Risk	rs61752129(C;C)
Alt	rs61752129(C;C)
Reference	Rs61752129(-;-)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 7A
Variation	info
Gene	PEX26
CLNDBN	Peroxisome biogenesis disorder 7A
Reversed	0
HGVS	NC_000022.10:g.18561176dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002237.2,