rs62507328

Orientation

minus

Stabilized

minus

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

Make rs62507328(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855286

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507328
dbSNP (classic)	rs62507328
ClinGen	rs62507328
ebi	rs62507328
HLI	rs62507328
Exac	rs62507328
Gnomad	rs62507328
Varsome	rs62507328
LitVar	rs62507328
Map	rs62507328
PheGenI	rs62507328
Biobank	rs62507328
1000 genomes	rs62507328
hgdp	rs62507328
ensembl	rs62507328
geneview	rs62507328
scholar	rs62507328
google	rs62507328
pharmgkb	rs62507328
gwascentral	rs62507328
openSNP	rs62507328
23andMe	rs62507328
SNPshot	rs62507328
SNPdbe	rs62507328
MSV3d	rs62507328
GWAS Ctlg	rs62507328

Max Magnitude

3

ClinVar
Risk	rs62507328(-;-)
Alt	rs62507328(-;-)
Reference	Rs62507328(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249064delT
CLNSRC
CLNACC	RCV000088982.1,