rs62508586

Orientation

minus

Stabilized

minus

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

Make rs62508586(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102877458

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508586
dbSNP (classic)	rs62508586
ClinGen	rs62508586
ebi	rs62508586
HLI	rs62508586
Exac	rs62508586
Gnomad	rs62508586
Varsome	rs62508586
LitVar	rs62508586
Map	rs62508586
PheGenI	rs62508586
Biobank	rs62508586
1000 genomes	rs62508586
hgdp	rs62508586
ensembl	rs62508586
geneview	rs62508586
scholar	rs62508586
google	rs62508586
pharmgkb	rs62508586
gwascentral	rs62508586
openSNP	rs62508586
23andMe	rs62508586
SNPshot	rs62508586
SNPdbe	rs62508586
MSV3d	rs62508586
GWAS Ctlg	rs62508586

Max Magnitude

3

ClinVar
Risk	rs62508586(G;G)
Alt	rs62508586(G;G)
Reference	Rs62508586(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103271236T>C
CLNSRC
CLNACC	RCV000088922.1,