rs61752138

Orientation

plus

Stabilized

plus

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

Make rs61752138(G;G)

Make rs61752138(G;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

7209700

Gene

PEX5

is a	snp
is	mentioned by
dbSNP	rs61752138
dbSNP (classic)	rs61752138
ClinGen	rs61752138
ebi	rs61752138
HLI	rs61752138
Exac	rs61752138
Gnomad	rs61752138
Varsome	rs61752138
LitVar	rs61752138
Map	rs61752138
PheGenI	rs61752138
Biobank	rs61752138
1000 genomes	rs61752138
hgdp	rs61752138
ensembl	rs61752138
geneview	rs61752138
scholar	rs61752138
google	rs61752138
pharmgkb	rs61752138
gwascentral	rs61752138
openSNP	rs61752138
23andMe	rs61752138
SNPshot	rs61752138
SNPdbe	rs61752138
MSV3d	rs61752138
GWAS Ctlg	rs61752138

Max Magnitude

0

OMIM	600414
Desc
Variant	0001
Related	also

ClinVar
Risk	rs61752138(G;G)
Alt	rs61752138(G;G)
Reference	Rs61752138(T;T)
Significance	Pathogenic
Disease	Neonatal adrenoleucodystrophy not provided
Variation	info
Gene	PEX5
CLNDBN	Neonatal adrenoleucodystrophy not provided
Reversed	0
HGVS	NC_000012.11:g.7362296T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009714.2, RCV000427819.1,