rs869312935

Orientation

minus

Stabilized

minus

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

Make rs869312935(C;C)

Make rs869312935(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

2406719

Gene

PEX10

is a	snp
is	mentioned by
dbSNP	rs869312935
dbSNP (classic)	rs869312935
ClinGen	rs869312935
ebi	rs869312935
HLI	rs869312935
Exac	rs869312935
Gnomad	rs869312935
Varsome	rs869312935
LitVar	rs869312935
Map	rs869312935
PheGenI	rs869312935
Biobank	rs869312935
1000 genomes	rs869312935
hgdp	rs869312935
ensembl	rs869312935
geneview	rs869312935
scholar	rs869312935
google	rs869312935
pharmgkb	rs869312935
gwascentral	rs869312935
openSNP	rs869312935
23andMe	rs869312935
SNPshot	rs869312935
SNPdbe	rs869312935
MSV3d	rs869312935
GWAS Ctlg	rs869312935

Max Magnitude

0

ClinVar
Risk	rs869312935(C;C)
Alt	rs869312935(C;C)
Reference	Rs869312935(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	PEX10
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000001.10:g.2338158C>G
CLNSRC
CLNACC	RCV000210672.1,