rs62508734

Orientation

minus

Stabilized

minus

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

Make rs62508734(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852818

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508734
dbSNP (classic)	rs62508734
ClinGen	rs62508734
ebi	rs62508734
HLI	rs62508734
Exac	rs62508734
Gnomad	rs62508734
Varsome	rs62508734
LitVar	rs62508734
Map	rs62508734
PheGenI	rs62508734
Biobank	rs62508734
1000 genomes	rs62508734
hgdp	rs62508734
ensembl	rs62508734
geneview	rs62508734
scholar	rs62508734
google	rs62508734
pharmgkb	rs62508734
gwascentral	rs62508734
openSNP	rs62508734
23andMe	rs62508734
SNPshot	rs62508734
SNPdbe	rs62508734
MSV3d	rs62508734
GWAS Ctlg	rs62508734

Max Magnitude

3

ClinVar
Risk	rs62508734(G;G)
Alt	rs62508734(G;G)
Reference	Rs62508734(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246596T>C
CLNSRC
CLNACC	RCV000089127.1,