rs62509017

Orientation

minus

Stabilized

minus

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

Make rs62509017(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102894846

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62509017
dbSNP (classic)	rs62509017
ClinGen	rs62509017
ebi	rs62509017
HLI	rs62509017
Exac	rs62509017
Gnomad	rs62509017
Varsome	rs62509017
LitVar	rs62509017
Map	rs62509017
PheGenI	rs62509017
Biobank	rs62509017
1000 genomes	rs62509017
hgdp	rs62509017
ensembl	rs62509017
geneview	rs62509017
scholar	rs62509017
google	rs62509017
pharmgkb	rs62509017
gwascentral	rs62509017
openSNP	rs62509017
23andMe	rs62509017
SNPshot	rs62509017
SNPdbe	rs62509017
MSV3d	rs62509017
GWAS Ctlg	rs62509017

Max Magnitude

3

ClinVar
Risk	rs62509017(C;C)
Alt	rs62509017(C;C)
Reference	Rs62509017(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103288624T>G
CLNSRC
CLNACC	RCV000088881.1,