rs62516063

Orientation

minus

Stabilized

minus

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

Make rs62516063(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102844363

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62516063
dbSNP (classic)	rs62516063
ClinGen	rs62516063
ebi	rs62516063
HLI	rs62516063
Exac	rs62516063
Gnomad	rs62516063
Varsome	rs62516063
LitVar	rs62516063
Map	rs62516063
PheGenI	rs62516063
Biobank	rs62516063
1000 genomes	rs62516063
hgdp	rs62516063
ensembl	rs62516063
geneview	rs62516063
scholar	rs62516063
google	rs62516063
pharmgkb	rs62516063
gwascentral	rs62516063
openSNP	rs62516063
23andMe	rs62516063
SNPshot	rs62516063
SNPdbe	rs62516063
MSV3d	rs62516063
GWAS Ctlg	rs62516063

Max Magnitude

3

ClinVar
Risk	rs62516063(-;-)
Alt	rs62516063(-;-)
Reference	Rs62516063(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103238141delC
CLNSRC
CLNACC	RCV000088718.1,