rs199475603

Orientation

minus

Stabilized

minus

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

Make rs199475603(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843646

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475603
dbSNP (classic)	rs199475603
ClinGen	rs199475603
ebi	rs199475603
HLI	rs199475603
Exac	rs199475603
Gnomad	rs199475603
Varsome	rs199475603
LitVar	rs199475603
Map	rs199475603
PheGenI	rs199475603
Biobank	rs199475603
1000 genomes	rs199475603
hgdp	rs199475603
ensembl	rs199475603
geneview	rs199475603
scholar	rs199475603
google	rs199475603
pharmgkb	rs199475603
gwascentral	rs199475603
openSNP	rs199475603
23andMe	rs199475603
SNPshot	rs199475603
SNPdbe	rs199475603
MSV3d	rs199475603
GWAS Ctlg	rs199475603

Max Magnitude

3

ClinVar
Risk	rs199475603(-;-)
Alt	rs199475603(-;-)
Reference	Rs199475603(TAAG;TAAG)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237424_103237427delCTTA
CLNSRC
CLNACC	RCV000088785.1,