rs35082957

Orientation

minus

Stabilized

minus

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

Make rs35082957(A;A)

Make rs35082957(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2406553

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs35082957
dbSNP (classic)	rs35082957
ClinGen	rs35082957
ebi	rs35082957
HLI	rs35082957
Exac	rs35082957
Gnomad	rs35082957
Varsome	rs35082957
LitVar	rs35082957
Map	rs35082957
PheGenI	rs35082957
Biobank	rs35082957
1000 genomes	rs35082957
hgdp	rs35082957
ensembl	rs35082957
geneview	rs35082957
scholar	rs35082957
google	rs35082957
pharmgkb	rs35082957
gwascentral	rs35082957
openSNP	rs35082957
23andMe	rs35082957
SNPshot	rs35082957
SNPdbe	rs35082957
MSV3d	rs35082957
GWAS Ctlg	rs35082957

GMAF

0.003214

Max Magnitude

0

ClinVar
Risk	rs35082957(A;A)
Alt	rs35082957(A;A)
Reference	Rs35082957(G;G)
Significance	Non-pathogenic
Disease	not specified Zellweger syndrome
Variation	info
Gene	PEX10
CLNDBN	not specified Zellweger syndrome
Reversed	1
HGVS	NC_000001.10:g.2337992C>T
CLNSRC	Illumina
CLNACC	RCV000247875.1, RCV000282889.1,