rs62507350

Orientation

minus

Stabilized

minus

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

Make rs62507350(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102844345

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507350
dbSNP (classic)	rs62507350
ClinGen	rs62507350
ebi	rs62507350
HLI	rs62507350
Exac	rs62507350
Gnomad	rs62507350
Varsome	rs62507350
LitVar	rs62507350
Map	rs62507350
PheGenI	rs62507350
Biobank	rs62507350
1000 genomes	rs62507350
hgdp	rs62507350
ensembl	rs62507350
geneview	rs62507350
scholar	rs62507350
google	rs62507350
pharmgkb	rs62507350
gwascentral	rs62507350
openSNP	rs62507350
23andMe	rs62507350
SNPshot	rs62507350
SNPdbe	rs62507350
MSV3d	rs62507350
GWAS Ctlg	rs62507350

Max Magnitude

3

ClinVar
Risk	rs62507350(-;-)
Alt	rs62507350(-;-)
Reference	Rs62507350(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103238123delA
CLNSRC
CLNACC	RCV000088730.1,