rs758020436

Orientation

plus

Stabilized

plus

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

Make rs758020436(C;T)

Make rs758020436(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

34992363

Gene

PDHX

is a	snp
is	mentioned by
dbSNP	rs758020436
dbSNP (classic)	rs758020436
ClinGen	rs758020436
ebi	rs758020436
HLI	rs758020436
Exac	rs758020436
Gnomad	rs758020436
Varsome	rs758020436
LitVar	rs758020436
Map	rs758020436
PheGenI	rs758020436
Biobank	rs758020436
1000 genomes	rs758020436
hgdp	rs758020436
ensembl	rs758020436
geneview	rs758020436
scholar	rs758020436
google	rs758020436
pharmgkb	rs758020436
gwascentral	rs758020436
openSNP	rs758020436
23andMe	rs758020436
SNPshot	rs758020436
SNPdbe	rs758020436
MSV3d	rs758020436
GWAS Ctlg	rs758020436

Max Magnitude

0

ClinVar
Risk	rs758020436(T;T)
Alt	rs758020436(T;T)
Reference	Rs758020436(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PDHX
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.35013910C>T
CLNSRC
CLNACC	RCV000196048.1,