rs1057518180

Orientation

plus

Stabilized

plus

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

Make rs1057518180(-;A)

Make rs1057518180(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

34966791

Gene

PDHX

is a	snp
is	mentioned by
dbSNP	rs1057518180
dbSNP (classic)	rs1057518180
ClinGen	rs1057518180
ebi	rs1057518180
HLI	rs1057518180
Exac	rs1057518180
Gnomad	rs1057518180
Varsome	rs1057518180
LitVar	rs1057518180
Map	rs1057518180
PheGenI	rs1057518180
Biobank	rs1057518180
1000 genomes	rs1057518180
hgdp	rs1057518180
ensembl	rs1057518180
geneview	rs1057518180
scholar	rs1057518180
google	rs1057518180
pharmgkb	rs1057518180
gwascentral	rs1057518180
openSNP	rs1057518180
23andMe	rs1057518180
SNPshot	rs1057518180
SNPdbe	rs1057518180
MSV3d	rs1057518180
GWAS Ctlg	rs1057518180

Max Magnitude

0

ClinVar
Risk	rs1057518180(A;A)
Alt	rs1057518180(A;A)
Reference	Rs1057518180(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PDHX
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.34988338dupA
CLNSRC
CLNACC	RCV000413565.1,