rs62642921

Orientation

minus

Stabilized

minus

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

Make rs62642921(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102843718

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62642921
dbSNP (classic)	rs62642921
ClinGen	rs62642921
ebi	rs62642921
HLI	rs62642921
Exac	rs62642921
Gnomad	rs62642921
Varsome	rs62642921
LitVar	rs62642921
Map	rs62642921
PheGenI	rs62642921
Biobank	rs62642921
1000 genomes	rs62642921
hgdp	rs62642921
ensembl	rs62642921
geneview	rs62642921
scholar	rs62642921
google	rs62642921
pharmgkb	rs62642921
gwascentral	rs62642921
openSNP	rs62642921
23andMe	rs62642921
SNPshot	rs62642921
SNPdbe	rs62642921
MSV3d	rs62642921
GWAS Ctlg	rs62642921

Max Magnitude

3

ClinVar
Risk	rs62642921(-;-)
Alt	rs62642921(-;-)
Reference	Rs62642921(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103237496delT
CLNSRC
CLNACC	RCV000088765.1,