rs199475666

Orientation

minus

Stabilized

minus

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

Make rs199475666(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102852920

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475666
dbSNP (classic)	rs199475666
ClinGen	rs199475666
ebi	rs199475666
HLI	rs199475666
Exac	rs199475666
Gnomad	rs199475666
Varsome	rs199475666
LitVar	rs199475666
Map	rs199475666
PheGenI	rs199475666
Biobank	rs199475666
1000 genomes	rs199475666
hgdp	rs199475666
ensembl	rs199475666
geneview	rs199475666
scholar	rs199475666
google	rs199475666
pharmgkb	rs199475666
gwascentral	rs199475666
openSNP	rs199475666
23andMe	rs199475666
SNPshot	rs199475666
SNPdbe	rs199475666
MSV3d	rs199475666
GWAS Ctlg	rs199475666

Max Magnitude

3

ClinVar
Risk	rs199475666(-;-)
Alt	rs199475666(-;-)
Reference	Rs199475666(C;C)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103246698delG
CLNSRC
CLNACC	RCV000089069.1,