rs62508620

Orientation

minus

Stabilized

minus

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

Make rs62508620(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843746

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508620
dbSNP (classic)	rs62508620
ClinGen	rs62508620
ebi	rs62508620
HLI	rs62508620
Exac	rs62508620
Gnomad	rs62508620
Varsome	rs62508620
LitVar	rs62508620
Map	rs62508620
PheGenI	rs62508620
Biobank	rs62508620
1000 genomes	rs62508620
hgdp	rs62508620
ensembl	rs62508620
geneview	rs62508620
scholar	rs62508620
google	rs62508620
pharmgkb	rs62508620
gwascentral	rs62508620
openSNP	rs62508620
23andMe	rs62508620
SNPshot	rs62508620
SNPdbe	rs62508620
MSV3d	rs62508620
GWAS Ctlg	rs62508620

Max Magnitude

3

ClinVar
Risk	rs62508620(-;-)
Alt	rs62508620(-;-)
Reference	Rs62508620(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237524delG
CLNSRC
CLNACC	RCV000088757.1,