rs62508649

Orientation

minus

Stabilized

minus

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

Make rs62508649(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102840396

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508649
dbSNP (classic)	rs62508649
ClinGen	rs62508649
ebi	rs62508649
HLI	rs62508649
Exac	rs62508649
Gnomad	rs62508649
Varsome	rs62508649
LitVar	rs62508649
Map	rs62508649
PheGenI	rs62508649
Biobank	rs62508649
1000 genomes	rs62508649
hgdp	rs62508649
ensembl	rs62508649
geneview	rs62508649
scholar	rs62508649
google	rs62508649
pharmgkb	rs62508649
gwascentral	rs62508649
openSNP	rs62508649
23andMe	rs62508649
SNPshot	rs62508649
SNPdbe	rs62508649
MSV3d	rs62508649
GWAS Ctlg	rs62508649

Max Magnitude

3

ClinVar
Risk	rs62508649(G;G)
Alt	rs62508649(G;G)
Reference	Rs62508649(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103234174T>C
CLNSRC
CLNACC	RCV000088828.1,