rs199475605

Orientation

minus

Stabilized

minus

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

Make rs199475605(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102877502

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475605
dbSNP (classic)	rs199475605
ClinGen	rs199475605
ebi	rs199475605
HLI	rs199475605
Exac	rs199475605
Gnomad	rs199475605
Varsome	rs199475605
LitVar	rs199475605
Map	rs199475605
PheGenI	rs199475605
Biobank	rs199475605
1000 genomes	rs199475605
hgdp	rs199475605
ensembl	rs199475605
geneview	rs199475605
scholar	rs199475605
google	rs199475605
pharmgkb	rs199475605
gwascentral	rs199475605
openSNP	rs199475605
23andMe	rs199475605
SNPshot	rs199475605
SNPdbe	rs199475605
MSV3d	rs199475605
GWAS Ctlg	rs199475605

Max Magnitude

3

ClinVar
Risk	rs199475605(-;-)
Alt	rs199475605(-;-)
Reference	Rs199475605(ATCA;ATCA)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103271280_103271283delTGAT
CLNSRC
CLNACC	RCV000088910.1,