rs199959402

Orientation

plus

Stabilized

plus

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

Make rs199959402(C;T)

Make rs199959402(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

19351368

Gene

PDHA1

is a	snp
is	mentioned by
dbSNP	rs199959402
dbSNP (classic)	rs199959402
ClinGen	rs199959402
ebi	rs199959402
HLI	rs199959402
Exac	rs199959402
Gnomad	rs199959402
Varsome	rs199959402
LitVar	rs199959402
Map	rs199959402
PheGenI	rs199959402
Biobank	rs199959402
1000 genomes	rs199959402
hgdp	rs199959402
ensembl	rs199959402
geneview	rs199959402
scholar	rs199959402
google	rs199959402
pharmgkb	rs199959402
gwascentral	rs199959402
openSNP	rs199959402
23andMe	rs199959402
SNPshot	rs199959402
SNPdbe	rs199959402
MSV3d	rs199959402
GWAS Ctlg	rs199959402

Max Magnitude

0

ClinVar
Risk	rs199959402(T;T)
Alt	rs199959402(T;T)
Reference	Rs199959402(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PDHA1
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.19369486C>T
CLNSRC
CLNACC	RCV000196836.1,