rs199475629

Orientation

minus

Stabilized

minus

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

Make rs199475629(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843681

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475629
dbSNP (classic)	rs199475629
ClinGen	rs199475629
ebi	rs199475629
HLI	rs199475629
Exac	rs199475629
Gnomad	rs199475629
Varsome	rs199475629
LitVar	rs199475629
Map	rs199475629
PheGenI	rs199475629
Biobank	rs199475629
1000 genomes	rs199475629
hgdp	rs199475629
ensembl	rs199475629
geneview	rs199475629
scholar	rs199475629
google	rs199475629
pharmgkb	rs199475629
gwascentral	rs199475629
openSNP	rs199475629
23andMe	rs199475629
SNPshot	rs199475629
SNPdbe	rs199475629
MSV3d	rs199475629
GWAS Ctlg	rs199475629

Max Magnitude

3

ClinVar
Risk	rs199475629(-;-)
Alt	rs199475629(-;-)
Reference	Rs199475629(TG;TG)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237459_103237460delCA
CLNSRC
CLNACC	RCV000088776.1,