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rs62517207

From SNPedia

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


Make rs62517207(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855283
GenePAH
is asnp
is mentioned by
dbSNPrs62517207
ebirs62517207
HLIrs62517207
Exacrs62517207
Varsomers62517207
Maprs62517207
PheGenIrs62517207
hapmaprs62517207
1000 genomesrs62517207
hgdprs62517207
ensemblrs62517207
gopubmedrs62517207
geneviewrs62517207
scholarrs62517207
googlers62517207
pharmgkbrs62517207
gwascentralrs62517207
openSNPrs62517207
23andMers62517207
23andMe allrs62517207
SNP Nexus

SNPshotrs62517207
SNPdbers62517207
MSV3drs62517207
GWAS Ctlgrs62517207
Max Magnitude3
ClinVar
Risk rs62517207(;)
Alt rs62517207(;)
Reference rs62517207(AT;AT)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103249061_103249062delAT
CLNSRC
CLNACC RCV000088983.1,