rs62507332

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;T)	3	Carrier of a phenylketonuria mutation

Make rs62507332(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102894856

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507332
dbSNP (classic)	rs62507332
ClinGen	rs62507332
ebi	rs62507332
HLI	rs62507332
Exac	rs62507332
Gnomad	rs62507332
Varsome	rs62507332
LitVar	rs62507332
Map	rs62507332
PheGenI	rs62507332
Biobank	rs62507332
1000 genomes	rs62507332
hgdp	rs62507332
ensembl	rs62507332
geneview	rs62507332
scholar	rs62507332
google	rs62507332
pharmgkb	rs62507332
gwascentral	rs62507332
openSNP	rs62507332
23andMe	rs62507332
SNPshot	rs62507332
SNPdbe	rs62507332
MSV3d	rs62507332
GWAS Ctlg	rs62507332

Max Magnitude

3

ClinVar
Risk	rs62507332(C;C) rs62507332(G;G)
Alt	rs62507332(C;C) rs62507332(G;G)
Reference	Rs62507332(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103288634A>C
CLNSRC
CLNACC	RCV000088879.1,