rs62508739

Orientation

minus

Stabilized

minus

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

Make rs62508739(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102851743

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508739
dbSNP (classic)	rs62508739
ClinGen	rs62508739
ebi	rs62508739
HLI	rs62508739
Exac	rs62508739
Gnomad	rs62508739
Varsome	rs62508739
LitVar	rs62508739
Map	rs62508739
PheGenI	rs62508739
Biobank	rs62508739
1000 genomes	rs62508739
hgdp	rs62508739
ensembl	rs62508739
geneview	rs62508739
scholar	rs62508739
google	rs62508739
pharmgkb	rs62508739
gwascentral	rs62508739
openSNP	rs62508739
23andMe	rs62508739
SNPshot	rs62508739
SNPdbe	rs62508739
MSV3d	rs62508739
GWAS Ctlg	rs62508739

Max Magnitude

3

ClinVar
Risk	rs62508739(A;A)
Alt	rs62508739(A;A)
Reference	Rs62508739(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103245521C>T
CLNSRC
CLNACC	RCV000089141.1,