rs1801152

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;C)	3	Carrier of a phenylketonuria mutation
(C;C)	0	common in clinvar

Make rs1801152(C;T)

Make rs1801152(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102840473

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs1801152
dbSNP (classic)	rs1801152
ClinGen	rs1801152
ebi	rs1801152
HLI	rs1801152
Exac	rs1801152
Gnomad	rs1801152
Varsome	rs1801152
LitVar	rs1801152
Map	rs1801152
PheGenI	rs1801152
Biobank	rs1801152
1000 genomes	rs1801152
hgdp	rs1801152
ensembl	rs1801152
geneview	rs1801152
scholar	rs1801152
google	rs1801152
pharmgkb	rs1801152
gwascentral	rs1801152
openSNP	rs1801152
23andMe	rs1801152
SNPshot	rs1801152
SNPdbe	rs1801152
MSV3d	rs1801152
GWAS Ctlg	rs1801152

Max Magnitude

3

ClinVar
Risk	rs1801152(T;T)
Alt	rs1801152(T;T)
Reference	Rs1801152(C;C)
Significance	Other
Disease	not provided not specified
Variation	info
Gene	PAH
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000012.11:g.103234251G>A
CLNSRC
CLNACC	RCV000088814.1, RCV000174235.3,