rs119463988

Orientation

plus

Stabilized

plus

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

Make rs119463988(G;G)

Make rs119463988(G;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

26735477

Gene

PDSS1

is a	snp
is	mentioned by
dbSNP	rs119463988
dbSNP (classic)	rs119463988
ClinGen	rs119463988
ebi	rs119463988
HLI	rs119463988
Exac	rs119463988
Gnomad	rs119463988
Varsome	rs119463988
LitVar	rs119463988
Map	rs119463988
PheGenI	rs119463988
Biobank	rs119463988
1000 genomes	rs119463988
hgdp	rs119463988
ensembl	rs119463988
geneview	rs119463988
scholar	rs119463988
google	rs119463988
pharmgkb	rs119463988
gwascentral	rs119463988
openSNP	rs119463988
23andMe	rs119463988
SNPshot	rs119463988
SNPdbe	rs119463988
MSV3d	rs119463988
GWAS Ctlg	rs119463988

Max Magnitude

0

OMIM	607429
Desc
Variant	0001
Related	also

ClinVar
Risk	rs119463988(G;G)
Alt	rs119463988(G;G)
Reference	Rs119463988(T;T)
Significance	Pathogenic
Disease	Coenzyme Q10 deficiency
Variation	info
Gene	PDSS1
CLNDBN	Coenzyme Q10 deficiency, primary, 2
Reversed	0
HGVS	NC_000010.10:g.27024406T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003393.3,