rs62517175

Orientation

minus

Stabilized

minus

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

Make rs62517175(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102866591

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62517175
dbSNP (classic)	rs62517175
ClinGen	rs62517175
ebi	rs62517175
HLI	rs62517175
Exac	rs62517175
Gnomad	rs62517175
Varsome	rs62517175
LitVar	rs62517175
Map	rs62517175
PheGenI	rs62517175
Biobank	rs62517175
1000 genomes	rs62517175
hgdp	rs62517175
ensembl	rs62517175
geneview	rs62517175
scholar	rs62517175
google	rs62517175
pharmgkb	rs62517175
gwascentral	rs62517175
openSNP	rs62517175
23andMe	rs62517175
SNPshot	rs62517175
SNPdbe	rs62517175
MSV3d	rs62517175
GWAS Ctlg	rs62517175

Max Magnitude

3

ClinVar
Risk	rs62517175(-;-)
Alt	rs62517175(-;-)
Reference	Rs62517175(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103260369delC
CLNSRC
CLNACC	RCV000088958.1,