rs281865437

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs281865437(C;C)

Make rs281865437(C;T)

Reference

GRCh38 38.1/142

Chromosome

12

Position

102840475

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs281865437
dbSNP (classic)	rs281865437
ClinGen	rs281865437
ebi	rs281865437
HLI	rs281865437
Exac	rs281865437
Gnomad	rs281865437
Varsome	rs281865437
LitVar	rs281865437
Map	rs281865437
PheGenI	rs281865437
Biobank	rs281865437
1000 genomes	rs281865437
hgdp	rs281865437
ensembl	rs281865437
geneview	rs281865437
scholar	rs281865437
google	rs281865437
pharmgkb	rs281865437
gwascentral	rs281865437
openSNP	rs281865437
23andMe	rs281865437
SNPshot	rs281865437
SNPdbe	rs281865437
MSV3d	rs281865437
GWAS Ctlg	rs281865437

Max Magnitude

0

ClinVar
Risk	rs281865437(C;C)
Alt	rs281865437(C;C)
Reference	Rs281865437(T;T)
Significance	Probable-Pathogenic
Disease	Phenylketonuria
Variation	info
Gene	PAH
CLNDBN	Phenylketonuria
Reversed	1
HGVS	NC_000012.11:g.103234253A>G
CLNSRC	ClinVar
CLNACC	RCV000106346.1,