rs138809906

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	3	Carrier of a phenylketonuria mutation

Make rs138809906(A;T)

Make rs138809906(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855321

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs138809906
dbSNP (classic)	rs138809906
ClinGen	rs138809906
ebi	rs138809906
HLI	rs138809906
Exac	rs138809906
Gnomad	rs138809906
Varsome	rs138809906
LitVar	rs138809906
Map	rs138809906
PheGenI	rs138809906
Biobank	rs138809906
1000 genomes	rs138809906
hgdp	rs138809906
ensembl	rs138809906
geneview	rs138809906
scholar	rs138809906
google	rs138809906
pharmgkb	rs138809906
gwascentral	rs138809906
openSNP	rs138809906
23andMe	rs138809906
SNPshot	rs138809906
SNPdbe	rs138809906
MSV3d	rs138809906
GWAS Ctlg	rs138809906

Max Magnitude

3

ClinVar
Risk	rs138809906(G;G) rs138809906(T;T)
Alt	rs138809906(G;G) rs138809906(T;T)
Reference	Rs138809906(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.103249099A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000088969.1,