rs1057517009

Orientation

minus

Stabilized

minus

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

Make rs1057517009(-;-)

Make rs1057517009(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

102852867

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs1057517009
dbSNP (classic)	rs1057517009
ClinGen	rs1057517009
ebi	rs1057517009
HLI	rs1057517009
Exac	rs1057517009
Gnomad	rs1057517009
Varsome	rs1057517009
LitVar	rs1057517009
Map	rs1057517009
PheGenI	rs1057517009
Biobank	rs1057517009
1000 genomes	rs1057517009
hgdp	rs1057517009
ensembl	rs1057517009
geneview	rs1057517009
scholar	rs1057517009
google	rs1057517009
pharmgkb	rs1057517009
gwascentral	rs1057517009
openSNP	rs1057517009
23andMe	rs1057517009
SNPshot	rs1057517009
SNPdbe	rs1057517009
MSV3d	rs1057517009
GWAS Ctlg	rs1057517009

Max Magnitude

0

ClinVar
Risk	rs1057517009(-;-)
Alt	rs1057517009(-;-)
Reference	Rs1057517009(C;C)
Significance	Probable-Pathogenic
Disease	Phenylketonuria
Variation	info
Gene	PAH
CLNDBN	Phenylketonuria
Reversed	1
HGVS	NC_000012.11:g.103246645delG
CLNSRC
CLNACC	RCV000409667.1,