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rs62507281

From SNPedia

Orientationminus
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)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855338
GenePAH
is asnp
is mentioned by
dbSNPrs62507281
ebirs62507281
HLIrs62507281
Exacrs62507281
Varsomers62507281
Maprs62507281
PheGenIrs62507281
hapmaprs62507281
1000 genomesrs62507281
hgdprs62507281
ensemblrs62507281
gopubmedrs62507281
geneviewrs62507281
scholarrs62507281
googlers62507281
pharmgkbrs62507281
gwascentralrs62507281
openSNPrs62507281
23andMers62507281
23andMe allrs62507281
SNP Nexus

SNPshotrs62507281
SNPdbers62507281
MSV3drs62507281
GWAS Ctlgrs62507281
Max Magnitude3
ClinVar
Risk rs62507281(A,G;A,G)
Alt rs62507281(A,G;A,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,