rs63102461

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	3	Carrier of a phenylketonuria mutation

Make rs63102461(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102866595

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs63102461
dbSNP (classic)	rs63102461
ClinGen	rs63102461
ebi	rs63102461
HLI	rs63102461
Exac	rs63102461
Gnomad	rs63102461
Varsome	rs63102461
LitVar	rs63102461
Map	rs63102461
PheGenI	rs63102461
Biobank	rs63102461
1000 genomes	rs63102461
hgdp	rs63102461
ensembl	rs63102461
geneview	rs63102461
scholar	rs63102461
google	rs63102461
pharmgkb	rs63102461
gwascentral	rs63102461
openSNP	rs63102461
23andMe	rs63102461
SNPshot	rs63102461
SNPdbe	rs63102461
MSV3d	rs63102461
GWAS Ctlg	rs63102461

Max Magnitude

3

ClinVar
Risk	rs63102461(A;A)
Alt	rs63102461(A;A)
Reference	Rs63102461(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103260373C>T
CLNSRC
CLNACC	RCV000088955.1,