rs199475591

Orientation

minus

Stabilized

minus

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

Make rs199475591(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102912822

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475591
dbSNP (classic)	rs199475591
ClinGen	rs199475591
ebi	rs199475591
HLI	rs199475591
Exac	rs199475591
Gnomad	rs199475591
Varsome	rs199475591
LitVar	rs199475591
Map	rs199475591
PheGenI	rs199475591
Biobank	rs199475591
1000 genomes	rs199475591
hgdp	rs199475591
ensembl	rs199475591
geneview	rs199475591
scholar	rs199475591
google	rs199475591
pharmgkb	rs199475591
gwascentral	rs199475591
openSNP	rs199475591
23andMe	rs199475591
SNPshot	rs199475591
SNPdbe	rs199475591
MSV3d	rs199475591
GWAS Ctlg	rs199475591

Max Magnitude

3

ClinVar
Risk	rs199475591(-;-)
Alt	rs199475591(-;-)
Reference	Rs199475591(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103306600delC
CLNSRC
CLNACC	RCV000088837.1,