rs61753236

Orientation

plus

Stabilized

plus

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

Make rs61753236(C;T)

Make rs61753236(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

136822739

Gene

PEX7

is a	snp
is	mentioned by
dbSNP	rs61753236
dbSNP (classic)	rs61753236
ClinGen	rs61753236
ebi	rs61753236
HLI	rs61753236
Exac	rs61753236
Gnomad	rs61753236
Varsome	rs61753236
LitVar	rs61753236
Map	rs61753236
PheGenI	rs61753236
Biobank	rs61753236
1000 genomes	rs61753236
hgdp	rs61753236
ensembl	rs61753236
geneview	rs61753236
scholar	rs61753236
google	rs61753236
pharmgkb	rs61753236
gwascentral	rs61753236
openSNP	rs61753236
23andMe	rs61753236
SNPshot	rs61753236
SNPdbe	rs61753236
MSV3d	rs61753236
GWAS Ctlg	rs61753236

Max Magnitude

0

ClinVar
Risk	rs61753236(T;T)
Alt	rs61753236(T;T)
Reference	Rs61753236(C;C)
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.137143877C>T
CLNSRC
CLNACC	RCV000169280.1,