rs61752103

Orientation

minus

Stabilized

minus

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

Make rs61752103(C;T)

Make rs61752103(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

35577180

Gene

PEX12

is a	snp
is	mentioned by
dbSNP	rs61752103
dbSNP (classic)	rs61752103
ClinGen	rs61752103
ebi	rs61752103
HLI	rs61752103
Exac	rs61752103
Gnomad	rs61752103
Varsome	rs61752103
LitVar	rs61752103
Map	rs61752103
PheGenI	rs61752103
Biobank	rs61752103
1000 genomes	rs61752103
hgdp	rs61752103
ensembl	rs61752103
geneview	rs61752103
scholar	rs61752103
google	rs61752103
pharmgkb	rs61752103
gwascentral	rs61752103
openSNP	rs61752103
23andMe	rs61752103
SNPshot	rs61752103
SNPdbe	rs61752103
MSV3d	rs61752103
GWAS Ctlg	rs61752103

Max Magnitude

0

OMIM	601758
Desc
Variant	0005
Related	also

ClinVar
Risk	rs61752103(G;G) rs61752103(T;T)
Alt	rs61752103(G;G) rs61752103(T;T)
Reference	Rs61752103(C;C)
Significance	Pathogenic
Disease	Peroxisome biogenesis disorder 3A Peroxisomal biogenesis disorder 3b
Variation	info
Gene	PEX12
CLNDBN	Peroxisome biogenesis disorder 3A Peroxisomal biogenesis disorder 3b
Reversed	1
HGVS	NC_000017.10:g.33904199G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008216.3, RCV000032926.4,