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rs62517175

From SNPedia

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


Make rs62517175(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102866591
GenePAH
is asnp
is mentioned by
dbSNPrs62517175
ebirs62517175
HLIrs62517175
Exacrs62517175
Varsomers62517175
Maprs62517175
PheGenIrs62517175
hapmaprs62517175
1000 genomesrs62517175
hgdprs62517175
ensemblrs62517175
gopubmedrs62517175
geneviewrs62517175
scholarrs62517175
googlers62517175
pharmgkbrs62517175
gwascentralrs62517175
openSNPrs62517175
23andMers62517175
23andMe allrs62517175
SNP Nexus

SNPshotrs62517175
SNPdbers62517175
MSV3drs62517175
GWAS Ctlgrs62517175
Max Magnitude3
ClinVar
Risk rs62517175(;)
Alt rs62517175(;)
Reference rs62517175(G;G)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103260369delC
CLNSRC
CLNACC RCV000088958.1,