rs886041874

Orientation

plus

Stabilized

plus

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

Chromosome

1

Position

119721323

Gene

PHGDH

is a	snp
is	mentioned by
dbSNP	rs886041874
dbSNP (classic)	rs886041874
ClinGen	rs886041874
ebi	rs886041874
HLI	rs886041874
Exac	rs886041874
Gnomad	rs886041874
Varsome	rs886041874
LitVar	rs886041874
Map	rs886041874
PheGenI	rs886041874
Biobank	rs886041874
1000 genomes	rs886041874
hgdp	rs886041874
ensembl	rs886041874
geneview	rs886041874
scholar	rs886041874
google	rs886041874
pharmgkb	rs886041874
gwascentral	rs886041874
openSNP	rs886041874
23andMe	rs886041874
SNPshot	rs886041874
SNPdbe	rs886041874
MSV3d	rs886041874
GWAS Ctlg	rs886041874

Max Magnitude

0

ClinVar
Risk	rs886041874(C;C)
Alt	rs886041874(C;C)
Reference	Rs886041874(T;T)
Significance	Pathogenic
Disease	not provided Epileptic encephalopathy Seizures
Variation	info
Gene	PHGDH
CLNDBN	not provided Epileptic encephalopathy Seizures
Reversed	0
HGVS	NC_000001.10:g.120263946T>C
CLNSRC
CLNACC	RCV000313790.1, RCV000415201.1,