rs62507264

Orientation

minus

Stabilized

minus

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

Make rs62507264(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102846956

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507264
dbSNP (classic)	rs62507264
ClinGen	rs62507264
ebi	rs62507264
HLI	rs62507264
Exac	rs62507264
Gnomad	rs62507264
Varsome	rs62507264
LitVar	rs62507264
Map	rs62507264
PheGenI	rs62507264
Biobank	rs62507264
1000 genomes	rs62507264
hgdp	rs62507264
ensembl	rs62507264
geneview	rs62507264
scholar	rs62507264
google	rs62507264
pharmgkb	rs62507264
gwascentral	rs62507264
openSNP	rs62507264
23andMe	rs62507264
SNPshot	rs62507264
SNPdbe	rs62507264
MSV3d	rs62507264
GWAS Ctlg	rs62507264

Max Magnitude

3

ClinVar
Risk	rs62507264(C;C) rs62507264(G;G)
Alt	rs62507264(C;C) rs62507264(G;G)
Reference	Rs62507264(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103240734A>C
CLNSRC
CLNACC	RCV000089155.1,