rs62508674

Orientation

minus

Stabilized

minus

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

Make rs62508674(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843641

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508674
dbSNP (classic)	rs62508674
ClinGen	rs62508674
ebi	rs62508674
HLI	rs62508674
Exac	rs62508674
Gnomad	rs62508674
Varsome	rs62508674
LitVar	rs62508674
Map	rs62508674
PheGenI	rs62508674
Biobank	rs62508674
1000 genomes	rs62508674
hgdp	rs62508674
ensembl	rs62508674
geneview	rs62508674
scholar	rs62508674
google	rs62508674
pharmgkb	rs62508674
gwascentral	rs62508674
openSNP	rs62508674
23andMe	rs62508674
SNPshot	rs62508674
SNPdbe	rs62508674
MSV3d	rs62508674
GWAS Ctlg	rs62508674

Max Magnitude

3

ClinVar
Risk	rs62508674(T;T)
Alt	rs62508674(T;T)
Reference	Rs62508674(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237419C>A
CLNSRC
CLNACC	RCV000088794.1,