rs199475676

Orientation

minus

Stabilized

minus

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

Make rs199475676(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852858

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475676
dbSNP (classic)	rs199475676
ClinGen	rs199475676
ebi	rs199475676
HLI	rs199475676
Exac	rs199475676
Gnomad	rs199475676
Varsome	rs199475676
LitVar	rs199475676
Map	rs199475676
PheGenI	rs199475676
Biobank	rs199475676
1000 genomes	rs199475676
hgdp	rs199475676
ensembl	rs199475676
geneview	rs199475676
scholar	rs199475676
google	rs199475676
pharmgkb	rs199475676
gwascentral	rs199475676
openSNP	rs199475676
23andMe	rs199475676
SNPshot	rs199475676
SNPdbe	rs199475676
MSV3d	rs199475676
GWAS Ctlg	rs199475676

Max Magnitude

3

ClinVar
Risk	rs199475676(G;G)
Alt	rs199475676(G;G)
Reference	Rs199475676(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246636G>C
CLNSRC
CLNACC	RCV000089098.1,