rs62507281

Orientation

minus

Stabilized

minus

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

Make rs62507281(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

102855338

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62507281
dbSNP (classic)	rs62507281
ClinGen	rs62507281
ebi	rs62507281
HLI	rs62507281
Exac	rs62507281
Gnomad	rs62507281
Varsome	rs62507281
LitVar	rs62507281
Map	rs62507281
PheGenI	rs62507281
Biobank	rs62507281
1000 genomes	rs62507281
hgdp	rs62507281
ensembl	rs62507281
geneview	rs62507281
scholar	rs62507281
google	rs62507281
pharmgkb	rs62507281
gwascentral	rs62507281
openSNP	rs62507281
23andMe	rs62507281
SNPshot	rs62507281
SNPdbe	rs62507281
MSV3d	rs62507281
GWAS Ctlg	rs62507281

Max Magnitude

3

ClinVar
Risk	rs62507281(A;A) rs62507281(G;G)
Alt	rs62507281(A;A) rs62507281(G;G)
Reference	Rs62507281(T;T)
Significance	Untested
Disease	not provided
Variation	info
Gene	PAH
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.103249116A>C; NC_000012.11:g.103249116A>T
CLNSRC
CLNACC	RCV000088962.1, RCV000088961.1,