rs62507261

Orientation

minus

Stabilized

minus

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

Make rs62507261(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102840523

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507261
dbSNP (classic)	rs62507261
ClinGen	rs62507261
ebi	rs62507261
HLI	rs62507261
Exac	rs62507261
Gnomad	rs62507261
Varsome	rs62507261
LitVar	rs62507261
Map	rs62507261
PheGenI	rs62507261
Biobank	rs62507261
1000 genomes	rs62507261
hgdp	rs62507261
ensembl	rs62507261
geneview	rs62507261
scholar	rs62507261
google	rs62507261
pharmgkb	rs62507261
gwascentral	rs62507261
openSNP	rs62507261
23andMe	rs62507261
SNPshot	rs62507261
SNPdbe	rs62507261
MSV3d	rs62507261
GWAS Ctlg	rs62507261

Max Magnitude

3

ClinVar
Risk	rs62507261(A;A) rs62507261(C;C) rs62507261(T;T)
Alt	rs62507261(A;A) rs62507261(C;C) rs62507261(T;T)
Reference	Rs62507261(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103234301C>T
CLNSRC
CLNACC	RCV000088799.1,