rs121909151

Orientation

plus

Stabilized

plus

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

Make rs121909151(C;T)

Make rs121909151(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

136869909

Gene

PEX7

is a	snp
is	mentioned by
dbSNP	rs121909151
dbSNP (classic)	rs121909151
ClinGen	rs121909151
ebi	rs121909151
HLI	rs121909151
Exac	rs121909151
Gnomad	rs121909151
Varsome	rs121909151
LitVar	rs121909151
Map	rs121909151
PheGenI	rs121909151
Biobank	rs121909151
1000 genomes	rs121909151
hgdp	rs121909151
ensembl	rs121909151
geneview	rs121909151
scholar	rs121909151
google	rs121909151
pharmgkb	rs121909151
gwascentral	rs121909151
openSNP	rs121909151
23andMe	rs121909151
SNPshot	rs121909151
SNPdbe	rs121909151
MSV3d	rs121909151
GWAS Ctlg	rs121909151

Max Magnitude

0

OMIM	601757
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909151(T;T)
Alt	rs121909151(T;T)
Reference	Rs121909151(C;C)
Significance	Pathogenic
Disease	Rhizomelic chondrodysplasia punctata type 1 Peroxisome biogenesis disorder 9B
Variation	info
Gene	PEX7
CLNDBN	Rhizomelic chondrodysplasia punctata type 1 Peroxisome biogenesis disorder 9B
Reversed	0
HGVS	NC_000006.11:g.137191047C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008223.5, RCV000032925.4,