rs62509018

Orientation

minus

Stabilized

minus

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

Make rs62509018(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843626

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62509018
dbSNP (classic)	rs62509018
ClinGen	rs62509018
ebi	rs62509018
HLI	rs62509018
Exac	rs62509018
Gnomad	rs62509018
Varsome	rs62509018
LitVar	rs62509018
Map	rs62509018
PheGenI	rs62509018
Biobank	rs62509018
1000 genomes	rs62509018
hgdp	rs62509018
ensembl	rs62509018
geneview	rs62509018
scholar	rs62509018
google	rs62509018
pharmgkb	rs62509018
gwascentral	rs62509018
openSNP	rs62509018
23andMe	rs62509018
SNPshot	rs62509018
SNPdbe	rs62509018
MSV3d	rs62509018
GWAS Ctlg	rs62509018

Max Magnitude

3

ClinVar
Risk	rs62509018(C;C)
Alt	rs62509018(C;C)
Reference	Rs62509018(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237404C>G
CLNSRC
CLNACC	RCV000088792.1,