rs1057520732

Orientation

minus

Stabilized

minus

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

Make rs1057520732(A;A)

Make rs1057520732(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

102851698

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs1057520732
dbSNP (classic)	rs1057520732
ClinGen	rs1057520732
ebi	rs1057520732
HLI	rs1057520732
Exac	rs1057520732
Gnomad	rs1057520732
Varsome	rs1057520732
LitVar	rs1057520732
Map	rs1057520732
PheGenI	rs1057520732
Biobank	rs1057520732
1000 genomes	rs1057520732
hgdp	rs1057520732
ensembl	rs1057520732
geneview	rs1057520732
scholar	rs1057520732
google	rs1057520732
pharmgkb	rs1057520732
gwascentral	rs1057520732
openSNP	rs1057520732
23andMe	rs1057520732
SNPshot	rs1057520732
SNPdbe	rs1057520732
MSV3d	rs1057520732
GWAS Ctlg	rs1057520732

Max Magnitude

0

ClinVar
Risk	rs1057520732(A;A)
Alt	rs1057520732(A;A)
Reference	Rs1057520732(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103245476G>T
CLNSRC
CLNACC	RCV000436688.1,