rs62507273

Orientation

minus

Stabilized

minus

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

Make rs62507273(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102844436

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507273
dbSNP (classic)	rs62507273
ClinGen	rs62507273
ebi	rs62507273
HLI	rs62507273
Exac	rs62507273
Gnomad	rs62507273
Varsome	rs62507273
LitVar	rs62507273
Map	rs62507273
PheGenI	rs62507273
Biobank	rs62507273
1000 genomes	rs62507273
hgdp	rs62507273
ensembl	rs62507273
geneview	rs62507273
scholar	rs62507273
google	rs62507273
pharmgkb	rs62507273
gwascentral	rs62507273
openSNP	rs62507273
23andMe	rs62507273
SNPshot	rs62507273
SNPdbe	rs62507273
MSV3d	rs62507273
GWAS Ctlg	rs62507273

Max Magnitude

3

ClinVar
Risk	rs62507273(A;A)
Alt	rs62507273(A;A)
Reference	Rs62507273(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103238214A>T
CLNSRC
CLNACC	RCV000089185.1,