rs62507274

Orientation

minus

Stabilized

minus

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

Make rs62507274(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102844437

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507274
dbSNP (classic)	rs62507274
ClinGen	rs62507274
ebi	rs62507274
HLI	rs62507274
Exac	rs62507274
Gnomad	rs62507274
Varsome	rs62507274
LitVar	rs62507274
Map	rs62507274
PheGenI	rs62507274
Biobank	rs62507274
1000 genomes	rs62507274
hgdp	rs62507274
ensembl	rs62507274
geneview	rs62507274
scholar	rs62507274
google	rs62507274
pharmgkb	rs62507274
gwascentral	rs62507274
openSNP	rs62507274
23andMe	rs62507274
SNPshot	rs62507274
SNPdbe	rs62507274
MSV3d	rs62507274
GWAS Ctlg	rs62507274

Max Magnitude

3

ClinVar
Risk	rs62507274(G;G)
Alt	rs62507274(G;G)
Reference	Rs62507274(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103238215A>C
CLNSRC
CLNACC	RCV000089186.1,