rs62508684

Orientation

minus

Stabilized

minus

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

Make rs62508684(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843780

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508684
dbSNP (classic)	rs62508684
ClinGen	rs62508684
ebi	rs62508684
HLI	rs62508684
Exac	rs62508684
Gnomad	rs62508684
Varsome	rs62508684
LitVar	rs62508684
Map	rs62508684
PheGenI	rs62508684
Biobank	rs62508684
1000 genomes	rs62508684
hgdp	rs62508684
ensembl	rs62508684
geneview	rs62508684
scholar	rs62508684
google	rs62508684
pharmgkb	rs62508684
gwascentral	rs62508684
openSNP	rs62508684
23andMe	rs62508684
SNPshot	rs62508684
SNPdbe	rs62508684
MSV3d	rs62508684
GWAS Ctlg	rs62508684

Max Magnitude

3

ClinVar
Risk	rs62508684(A;A)
Alt	rs62508684(A;A)
Reference	Rs62508684(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237558C>T
CLNSRC
CLNACC	RCV000088740.1,