rs786205556

Orientation

plus

Stabilized

plus

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

Make rs786205556(C;T)

Make rs786205556(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

22

Position

18078604

Gene

PEX26

is a	snp
is	mentioned by
dbSNP	rs786205556
dbSNP (classic)	rs786205556
ClinGen	rs786205556
ebi	rs786205556
HLI	rs786205556
Exac	rs786205556
Gnomad	rs786205556
Varsome	rs786205556
LitVar	rs786205556
Map	rs786205556
PheGenI	rs786205556
Biobank	rs786205556
1000 genomes	rs786205556
hgdp	rs786205556
ensembl	rs786205556
geneview	rs786205556
scholar	rs786205556
google	rs786205556
pharmgkb	rs786205556
gwascentral	rs786205556
openSNP	rs786205556
23andMe	rs786205556
SNPshot	rs786205556
SNPdbe	rs786205556
MSV3d	rs786205556
GWAS Ctlg	rs786205556

Max Magnitude

0

ClinVar
Risk	rs786205556(T;T)
Alt	rs786205556(T;T)
Reference	Rs786205556(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PEX26
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.18561370C>T
CLNSRC
CLNACC	RCV000171354.1,