rs63083560

Orientation

minus

Stabilized

minus

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

Make rs63083560(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855229

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs63083560
dbSNP (classic)	rs63083560
ClinGen	rs63083560
ebi	rs63083560
HLI	rs63083560
Exac	rs63083560
Gnomad	rs63083560
Varsome	rs63083560
LitVar	rs63083560
Map	rs63083560
PheGenI	rs63083560
Biobank	rs63083560
1000 genomes	rs63083560
hgdp	rs63083560
ensembl	rs63083560
geneview	rs63083560
scholar	rs63083560
google	rs63083560
pharmgkb	rs63083560
gwascentral	rs63083560
openSNP	rs63083560
23andMe	rs63083560
SNPshot	rs63083560
SNPdbe	rs63083560
MSV3d	rs63083560
GWAS Ctlg	rs63083560

Max Magnitude

3

ClinVar
Risk	rs63083560(A;A)
Alt	rs63083560(A;A)
Reference	Rs63083560(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249007C>T
CLNSRC
CLNACC	RCV000089009.1,