rs63749677

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;ACCCATTTGGATAAAC)	3	Possibly a carrier of a phenylketonuria mutation
(ACCCATTTGGATAAAC;ACCCATTTGGATAAAC)	0	common in clinvar

Make rs63749677(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102894831

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs63749677
dbSNP (classic)	rs63749677
ClinGen	rs63749677
ebi	rs63749677
HLI	rs63749677
Exac	rs63749677
Gnomad	rs63749677
Varsome	rs63749677
LitVar	rs63749677
Map	rs63749677
PheGenI	rs63749677
Biobank	rs63749677
1000 genomes	rs63749677
hgdp	rs63749677
ensembl	rs63749677
geneview	rs63749677
scholar	rs63749677
google	rs63749677
pharmgkb	rs63749677
gwascentral	rs63749677
openSNP	rs63749677
23andMe	rs63749677
SNPshot	rs63749677
SNPdbe	rs63749677
MSV3d	rs63749677
GWAS Ctlg	rs63749677

Max Magnitude

3

ClinVar
Risk	rs63749677(-;-)
Alt	rs63749677(-;-)
Reference	Rs63749677(ACCCATTTGGATAAAC;ACCCATTTGGATAAAC)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103288609_103288624del16
CLNSRC
CLNACC	RCV000088882.1,