rs62509019

Orientation

minus

Stabilized

minus

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

Make rs62509019(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102851758

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62509019
dbSNP (classic)	rs62509019
ClinGen	rs62509019
ebi	rs62509019
HLI	rs62509019
Exac	rs62509019
Gnomad	rs62509019
Varsome	rs62509019
LitVar	rs62509019
Map	rs62509019
PheGenI	rs62509019
Biobank	rs62509019
1000 genomes	rs62509019
hgdp	rs62509019
ensembl	rs62509019
geneview	rs62509019
scholar	rs62509019
google	rs62509019
pharmgkb	rs62509019
gwascentral	rs62509019
openSNP	rs62509019
23andMe	rs62509019
SNPshot	rs62509019
SNPdbe	rs62509019
MSV3d	rs62509019
GWAS Ctlg	rs62509019

Max Magnitude

3

ClinVar
Risk	rs62509019(T;T)
Alt	rs62509019(T;T)
Reference	Rs62509019(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103245536T>A
CLNSRC
CLNACC	RCV000089134.1,