rs62507334

Orientation

minus

Stabilized

minus

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

Make rs62507334(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843793

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507334
dbSNP (classic)	rs62507334
ClinGen	rs62507334
ebi	rs62507334
HLI	rs62507334
Exac	rs62507334
Gnomad	rs62507334
Varsome	rs62507334
LitVar	rs62507334
Map	rs62507334
PheGenI	rs62507334
Biobank	rs62507334
1000 genomes	rs62507334
hgdp	rs62507334
ensembl	rs62507334
geneview	rs62507334
scholar	rs62507334
google	rs62507334
pharmgkb	rs62507334
gwascentral	rs62507334
openSNP	rs62507334
23andMe	rs62507334
SNPshot	rs62507334
SNPdbe	rs62507334
MSV3d	rs62507334
GWAS Ctlg	rs62507334

Max Magnitude

3

ClinVar
Risk	rs62507334(G;G) rs62507334(T;T)
Alt	rs62507334(G;G) rs62507334(T;T)
Reference	Rs62507334(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237571G>C
CLNSRC
CLNACC	RCV000088739.1,