rs199475656

Orientation

minus

Stabilized

minus

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

Make rs199475656(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855138

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475656
dbSNP (classic)	rs199475656
ClinGen	rs199475656
ebi	rs199475656
HLI	rs199475656
Exac	rs199475656
Gnomad	rs199475656
Varsome	rs199475656
LitVar	rs199475656
Map	rs199475656
PheGenI	rs199475656
Biobank	rs199475656
1000 genomes	rs199475656
hgdp	rs199475656
ensembl	rs199475656
geneview	rs199475656
scholar	rs199475656
google	rs199475656
pharmgkb	rs199475656
gwascentral	rs199475656
openSNP	rs199475656
23andMe	rs199475656
SNPshot	rs199475656
SNPdbe	rs199475656
MSV3d	rs199475656
GWAS Ctlg	rs199475656

Max Magnitude

3

ClinVar
Risk	rs199475656(C;C)
Alt	rs199475656(C;C)
Reference	Rs199475656(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103248916T>G
CLNSRC
CLNACC	RCV000089042.1,