rs62507335

Orientation

minus

Stabilized

minus

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

Make rs62507335(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852863

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507335
dbSNP (classic)	rs62507335
ClinGen	rs62507335
ebi	rs62507335
HLI	rs62507335
Exac	rs62507335
Gnomad	rs62507335
Varsome	rs62507335
LitVar	rs62507335
Map	rs62507335
PheGenI	rs62507335
Biobank	rs62507335
1000 genomes	rs62507335
hgdp	rs62507335
ensembl	rs62507335
geneview	rs62507335
scholar	rs62507335
google	rs62507335
pharmgkb	rs62507335
gwascentral	rs62507335
openSNP	rs62507335
23andMe	rs62507335
SNPshot	rs62507335
SNPdbe	rs62507335
MSV3d	rs62507335
GWAS Ctlg	rs62507335

Max Magnitude

3

ClinVar
Risk	rs62507335(A;A)
Alt	rs62507335(A;A)
Reference	Rs62507335(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246641C>T
CLNSRC
CLNACC	RCV000089095.1,