rs61753245

Orientation

plus

Stabilized

plus

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

Make rs61753245(A;A)

Make rs61753245(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

136866718

Gene

PEX7

is a	snp
is	mentioned by
dbSNP	rs61753245
dbSNP (classic)	rs61753245
ClinGen	rs61753245
ebi	rs61753245
HLI	rs61753245
Exac	rs61753245
Gnomad	rs61753245
Varsome	rs61753245
LitVar	rs61753245
Map	rs61753245
PheGenI	rs61753245
Biobank	rs61753245
1000 genomes	rs61753245
hgdp	rs61753245
ensembl	rs61753245
geneview	rs61753245
scholar	rs61753245
google	rs61753245
pharmgkb	rs61753245
gwascentral	rs61753245
openSNP	rs61753245
23andMe	rs61753245
SNPshot	rs61753245
SNPdbe	rs61753245
MSV3d	rs61753245
GWAS Ctlg	rs61753245

Max Magnitude

0

ClinVar
Risk	rs61753245(A;A)
Alt	rs61753245(A;A)
Reference	Rs61753245(G;G)
Significance	Probable-Pathogenic
Disease	Rhizomelic chondrodysplasia punctata type 1
Variation	info
Gene	PEX7
CLNDBN	Rhizomelic chondrodysplasia punctata type 1
Reversed	0
HGVS	NC_000006.11:g.137187856G>A
CLNSRC
CLNACC	RCV000169479.1,