rs62642910

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;G)	3	Carrier of a phenylketonuria mutation

Make rs62642910(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102851715

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62642910
dbSNP (classic)	rs62642910
ClinGen	rs62642910
ebi	rs62642910
HLI	rs62642910
Exac	rs62642910
Gnomad	rs62642910
Varsome	rs62642910
LitVar	rs62642910
Map	rs62642910
PheGenI	rs62642910
Biobank	rs62642910
1000 genomes	rs62642910
hgdp	rs62642910
ensembl	rs62642910
geneview	rs62642910
scholar	rs62642910
google	rs62642910
pharmgkb	rs62642910
gwascentral	rs62642910
openSNP	rs62642910
23andMe	rs62642910
SNPshot	rs62642910
SNPdbe	rs62642910
MSV3d	rs62642910
GWAS Ctlg	rs62642910

Max Magnitude

3

ClinVar
Risk	rs62642910(G;G)
Alt	rs62642910(G;G)
Reference	Rs62642910(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103245493G>C
CLNSRC
CLNACC	RCV000089145.1,