rs63083561

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;23)	3	Carrier of a phenylketonuria mutation
(TGTATAAAACCCATGCTTGCTAT;TGTATAAAACCCATGCTTGCTAT)	0	common in clinvar

Make rs63083561(-;-)

Make rs63083561(-;TGTATAAAACCCATGCTTGCTAT)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855230

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs63083561
dbSNP (classic)	rs63083561
ClinGen	rs63083561
ebi	rs63083561
HLI	rs63083561
Exac	rs63083561
Gnomad	rs63083561
Varsome	rs63083561
LitVar	rs63083561
Map	rs63083561
PheGenI	rs63083561
Biobank	rs63083561
1000 genomes	rs63083561
hgdp	rs63083561
ensembl	rs63083561
geneview	rs63083561
scholar	rs63083561
google	rs63083561
pharmgkb	rs63083561
gwascentral	rs63083561
openSNP	rs63083561
23andMe	rs63083561
SNPshot	rs63083561
SNPdbe	rs63083561
MSV3d	rs63083561
GWAS Ctlg	rs63083561

Max Magnitude

3

ClinVar
Risk	rs63083561(-;-)
Alt	rs63083561(-;-)
Reference	Rs63083561(TGTATAAAACCCATGCTTGCTAT;TGTATAAAACCCATGCTTGCTAT)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249008_103249030del23
CLNSRC
CLNACC	RCV000088994.1,