rs199475681

Orientation

minus

Stabilized

minus

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

Make rs199475681(G;T)

Make rs199475681(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

102877535

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs199475681
dbSNP (classic)	rs199475681
ClinGen	rs199475681
ebi	rs199475681
HLI	rs199475681
Exac	rs199475681
Gnomad	rs199475681
Varsome	rs199475681
LitVar	rs199475681
Map	rs199475681
PheGenI	rs199475681
Biobank	rs199475681
1000 genomes	rs199475681
hgdp	rs199475681
ensembl	rs199475681
geneview	rs199475681
scholar	rs199475681
google	rs199475681
pharmgkb	rs199475681
gwascentral	rs199475681
openSNP	rs199475681
23andMe	rs199475681
SNPshot	rs199475681
SNPdbe	rs199475681
MSV3d	rs199475681
GWAS Ctlg	rs199475681

Max Magnitude

0

ClinVar
Risk	rs199475681(T;T)
Alt	rs199475681(T;T)
Reference	Rs199475681(G;G)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103271313C>A
CLNSRC
CLNACC	RCV000088905.3,