rs786205502

Orientation

minus

Stabilized

minus

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

Make rs786205502(C;T)

Make rs786205502(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

35577102

Gene

PEX12

is a	snp
is	mentioned by
dbSNP	rs786205502
dbSNP (classic)	rs786205502
ClinGen	rs786205502
ebi	rs786205502
HLI	rs786205502
Exac	rs786205502
Gnomad	rs786205502
Varsome	rs786205502
LitVar	rs786205502
Map	rs786205502
PheGenI	rs786205502
Biobank	rs786205502
1000 genomes	rs786205502
hgdp	rs786205502
ensembl	rs786205502
geneview	rs786205502
scholar	rs786205502
google	rs786205502
pharmgkb	rs786205502
gwascentral	rs786205502
openSNP	rs786205502
23andMe	rs786205502
SNPshot	rs786205502
SNPdbe	rs786205502
MSV3d	rs786205502
GWAS Ctlg	rs786205502

Max Magnitude

0

ClinVar
Risk	rs786205502(T;T)
Alt	rs786205502(T;T)
Reference	Rs786205502(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PEX12
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.33904121G>A
CLNSRC
CLNACC	RCV000171253.1,