rs745949756

Orientation

plus

Stabilized

plus

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

Make rs745949756(A;G)

Make rs745949756(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

34994922

Gene

PDHX

is a	snp
is	mentioned by
dbSNP	rs745949756
dbSNP (classic)	rs745949756
ClinGen	rs745949756
ebi	rs745949756
HLI	rs745949756
Exac	rs745949756
Gnomad	rs745949756
Varsome	rs745949756
LitVar	rs745949756
Map	rs745949756
PheGenI	rs745949756
Biobank	rs745949756
1000 genomes	rs745949756
hgdp	rs745949756
ensembl	rs745949756
geneview	rs745949756
scholar	rs745949756
google	rs745949756
pharmgkb	rs745949756
gwascentral	rs745949756
openSNP	rs745949756
23andMe	rs745949756
SNPshot	rs745949756
SNPdbe	rs745949756
MSV3d	rs745949756
GWAS Ctlg	rs745949756

Max Magnitude

0

ClinVar
Risk	rs745949756(G;G)
Alt	rs745949756(G;G)
Reference	Rs745949756(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PDHX
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.35016469A>G
CLNSRC
CLNACC	RCV000197652.2,