rs62508650

Orientation

minus

Stabilized

minus

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

Make rs62508650(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102840394

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508650
dbSNP (classic)	rs62508650
ClinGen	rs62508650
ebi	rs62508650
HLI	rs62508650
Exac	rs62508650
Gnomad	rs62508650
Varsome	rs62508650
LitVar	rs62508650
Map	rs62508650
PheGenI	rs62508650
Biobank	rs62508650
1000 genomes	rs62508650
hgdp	rs62508650
ensembl	rs62508650
geneview	rs62508650
scholar	rs62508650
google	rs62508650
pharmgkb	rs62508650
gwascentral	rs62508650
openSNP	rs62508650
23andMe	rs62508650
SNPshot	rs62508650
SNPdbe	rs62508650
MSV3d	rs62508650
GWAS Ctlg	rs62508650

Max Magnitude

3

ClinVar
Risk	rs62508650(A;A)
Alt	rs62508650(A;A)
Reference	Rs62508650(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103234172A>T
CLNSRC
CLNACC	RCV000088829.1,