rs63749676

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;22)	3	Carrier of a phenylketonuria mutation
(ATAAAACCCATGCTTGCTATGA;ATAAAACCCATGCTTGCTATGA)	0	common in clinvar

Make rs63749676(-;-)

Make rs63749676(-;ATAAAACCCATGCTTGCTATGA)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855228

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs63749676
dbSNP (classic)	rs63749676
ClinGen	rs63749676
ebi	rs63749676
HLI	rs63749676
Exac	rs63749676
Gnomad	rs63749676
Varsome	rs63749676
LitVar	rs63749676
Map	rs63749676
PheGenI	rs63749676
Biobank	rs63749676
1000 genomes	rs63749676
hgdp	rs63749676
ensembl	rs63749676
geneview	rs63749676
scholar	rs63749676
google	rs63749676
pharmgkb	rs63749676
gwascentral	rs63749676
openSNP	rs63749676
23andMe	rs63749676
SNPshot	rs63749676
SNPdbe	rs63749676
MSV3d	rs63749676
GWAS Ctlg	rs63749676

Max Magnitude

3

ClinVar
Risk	rs63749676(-;-)
Alt	rs63749676(-;-)
Reference	Rs63749676(ATAAAACCCATGCTTGCTATGA;ATAAAACCCATGCTTGCTATGA)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249006_103249027del22
CLNSRC
CLNACC	RCV000088996.1,