rs62507260

Orientation

minus

Stabilized

minus

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

Make rs62507260(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855279

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507260
dbSNP (classic)	rs62507260
ClinGen	rs62507260
ebi	rs62507260
HLI	rs62507260
Exac	rs62507260
Gnomad	rs62507260
Varsome	rs62507260
LitVar	rs62507260
Map	rs62507260
PheGenI	rs62507260
Biobank	rs62507260
1000 genomes	rs62507260
hgdp	rs62507260
ensembl	rs62507260
geneview	rs62507260
scholar	rs62507260
google	rs62507260
pharmgkb	rs62507260
gwascentral	rs62507260
openSNP	rs62507260
23andMe	rs62507260
SNPshot	rs62507260
SNPdbe	rs62507260
MSV3d	rs62507260
GWAS Ctlg	rs62507260

Max Magnitude

3

ClinVar
Risk	rs62507260(-;-)
Alt	rs62507260(-;-)
Reference	Rs62507260(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249057delC
CLNSRC
CLNACC	RCV000088988.1,