rs199475668

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;8)	3	Carrier of a phenylketonuria mutation
(GAACCGTG;GAACCGTG)	0	common in clinvar

Make rs199475668(-;-)

Make rs199475668(-;GAACCGTG)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852812

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475668
dbSNP (classic)	rs199475668
ClinGen	rs199475668
ebi	rs199475668
HLI	rs199475668
Exac	rs199475668
Gnomad	rs199475668
Varsome	rs199475668
LitVar	rs199475668
Map	rs199475668
PheGenI	rs199475668
Biobank	rs199475668
1000 genomes	rs199475668
hgdp	rs199475668
ensembl	rs199475668
geneview	rs199475668
scholar	rs199475668
google	rs199475668
pharmgkb	rs199475668
gwascentral	rs199475668
openSNP	rs199475668
23andMe	rs199475668
SNPshot	rs199475668
SNPdbe	rs199475668
MSV3d	rs199475668
GWAS Ctlg	rs199475668

Max Magnitude

3

ClinVar
Risk	rs199475668(-;-)
Alt	rs199475668(-;-)
Reference	Rs199475668(GAACCGTG;GAACCGTG)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246590_103246597delCACGGTTC
CLNSRC
CLNACC	RCV000089126.1,