rs62507341

Orientation

minus

Stabilized

minus

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

Make rs62507341(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102894931

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507341
dbSNP (classic)	rs62507341
ClinGen	rs62507341
ebi	rs62507341
HLI	rs62507341
Exac	rs62507341
Gnomad	rs62507341
Varsome	rs62507341
LitVar	rs62507341
Map	rs62507341
PheGenI	rs62507341
Biobank	rs62507341
1000 genomes	rs62507341
hgdp	rs62507341
ensembl	rs62507341
geneview	rs62507341
scholar	rs62507341
google	rs62507341
pharmgkb	rs62507341
gwascentral	rs62507341
openSNP	rs62507341
23andMe	rs62507341
SNPshot	rs62507341
SNPdbe	rs62507341
MSV3d	rs62507341
GWAS Ctlg	rs62507341

Max Magnitude

3

ClinVar
Risk	rs62507341(G;G)
Alt	rs62507341(G;G)
Reference	Rs62507341(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103288709A>C
CLNSRC
CLNACC	RCV000088853.1,