rs62508737

Orientation

minus

Stabilized

minus

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

Make rs62508737(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843644

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508737
dbSNP (classic)	rs62508737
ClinGen	rs62508737
ebi	rs62508737
HLI	rs62508737
Exac	rs62508737
Gnomad	rs62508737
Varsome	rs62508737
LitVar	rs62508737
Map	rs62508737
PheGenI	rs62508737
Biobank	rs62508737
1000 genomes	rs62508737
hgdp	rs62508737
ensembl	rs62508737
geneview	rs62508737
scholar	rs62508737
google	rs62508737
pharmgkb	rs62508737
gwascentral	rs62508737
openSNP	rs62508737
23andMe	rs62508737
SNPshot	rs62508737
SNPdbe	rs62508737
MSV3d	rs62508737
GWAS Ctlg	rs62508737

Max Magnitude

3

ClinVar
Risk	rs62508737(C;C)
Alt	rs62508737(C;C)
Reference	Rs62508737(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237422A>G
CLNSRC
CLNACC	RCV000088793.1,