rs62507286

Orientation

minus

Stabilized

minus

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

Make rs62507286(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852843

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507286
dbSNP (classic)	rs62507286
ClinGen	rs62507286
ebi	rs62507286
HLI	rs62507286
Exac	rs62507286
Gnomad	rs62507286
Varsome	rs62507286
LitVar	rs62507286
Map	rs62507286
PheGenI	rs62507286
Biobank	rs62507286
1000 genomes	rs62507286
hgdp	rs62507286
ensembl	rs62507286
geneview	rs62507286
scholar	rs62507286
google	rs62507286
pharmgkb	rs62507286
gwascentral	rs62507286
openSNP	rs62507286
23andMe	rs62507286
SNPshot	rs62507286
SNPdbe	rs62507286
MSV3d	rs62507286
GWAS Ctlg	rs62507286

Max Magnitude

3

ClinVar
Risk	rs62507286(-;-)
Alt	rs62507286(-;-)
Reference	Rs62507286(ACATG;ACATG)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246621_103246625delCATGT
CLNSRC
CLNACC	RCV000089107.1,