rs62507269

Orientation

minus

Stabilized

minus

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

Make rs62507269(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852951

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507269
dbSNP (classic)	rs62507269
ClinGen	rs62507269
ebi	rs62507269
HLI	rs62507269
Exac	rs62507269
Gnomad	rs62507269
Varsome	rs62507269
LitVar	rs62507269
Map	rs62507269
PheGenI	rs62507269
Biobank	rs62507269
1000 genomes	rs62507269
hgdp	rs62507269
ensembl	rs62507269
geneview	rs62507269
scholar	rs62507269
google	rs62507269
pharmgkb	rs62507269
gwascentral	rs62507269
openSNP	rs62507269
23andMe	rs62507269
SNPshot	rs62507269
SNPdbe	rs62507269
MSV3d	rs62507269
GWAS Ctlg	rs62507269

Max Magnitude

3

ClinVar
Risk	rs62507269(A;A)
Alt	rs62507269(A;A)
Reference	Rs62507269(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246729C>T
CLNSRC
CLNACC	RCV000089044.1,