rs62895363

Orientation

minus

Stabilized

minus

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

Make rs62895363(-;-)

Make rs62895363(-;TCCTTGTATAAAACCCATGCTTG)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855234

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62895363
dbSNP (classic)	rs62895363
ClinGen	rs62895363
ebi	rs62895363
HLI	rs62895363
Exac	rs62895363
Gnomad	rs62895363
Varsome	rs62895363
LitVar	rs62895363
Map	rs62895363
PheGenI	rs62895363
Biobank	rs62895363
1000 genomes	rs62895363
hgdp	rs62895363
ensembl	rs62895363
geneview	rs62895363
scholar	rs62895363
google	rs62895363
pharmgkb	rs62895363
gwascentral	rs62895363
openSNP	rs62895363
23andMe	rs62895363
SNPshot	rs62895363
SNPdbe	rs62895363
MSV3d	rs62895363
GWAS Ctlg	rs62895363

Max Magnitude

3

ClinVar
Risk	rs62895363(-;-)
Alt	rs62895363(-;-)
Reference	Rs62895363(TCCTTGTATAAAACCCATGCTTG;TCCTTGTATAAAACCCATGCTTG)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249012_103249034del23
CLNSRC
CLNACC	RCV000088992.1,