rs62516099

Orientation

minus

Stabilized

minus

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

Make rs62516099(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843727

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62516099
dbSNP (classic)	rs62516099
ClinGen	rs62516099
ebi	rs62516099
HLI	rs62516099
Exac	rs62516099
Gnomad	rs62516099
Varsome	rs62516099
LitVar	rs62516099
Map	rs62516099
PheGenI	rs62516099
Biobank	rs62516099
1000 genomes	rs62516099
hgdp	rs62516099
ensembl	rs62516099
geneview	rs62516099
scholar	rs62516099
google	rs62516099
pharmgkb	rs62516099
gwascentral	rs62516099
openSNP	rs62516099
23andMe	rs62516099
SNPshot	rs62516099
SNPdbe	rs62516099
MSV3d	rs62516099
GWAS Ctlg	rs62516099

Max Magnitude

3

ClinVar
Risk	rs62516099(-;-)
Alt	rs62516099(-;-)
Reference	Rs62516099(GC;GC)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237505_103237506delGC
CLNSRC
CLNACC	RCV000088763.1,