rs62508688

Orientation

minus

Stabilized

minus

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

Make rs62508688(C;C)

Make rs62508688(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102844365

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508688
dbSNP (classic)	rs62508688
ClinGen	rs62508688
ebi	rs62508688
HLI	rs62508688
Exac	rs62508688
Gnomad	rs62508688
Varsome	rs62508688
LitVar	rs62508688
Map	rs62508688
PheGenI	rs62508688
Biobank	rs62508688
1000 genomes	rs62508688
hgdp	rs62508688
ensembl	rs62508688
geneview	rs62508688
scholar	rs62508688
google	rs62508688
pharmgkb	rs62508688
gwascentral	rs62508688
openSNP	rs62508688
23andMe	rs62508688
SNPshot	rs62508688
SNPdbe	rs62508688
MSV3d	rs62508688
GWAS Ctlg	rs62508688

Max Magnitude

3

ClinVar
Risk	rs62508688(A;A) rs62508688(C;C)
Alt	rs62508688(A;A) rs62508688(C;C)
Reference	Rs62508688(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103238143C>G; NC_000012.11:g.103238143C>T
CLNSRC
CLNACC	RCV000088717.1, RCV000088716.1,