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rs62514909

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62514909(C;G)
Make rs62514909(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102866668
GenePAH
is asnp
is mentioned by
dbSNPrs62514909
ebirs62514909
HLIrs62514909
Exacrs62514909
Varsomers62514909
Maprs62514909
PheGenIrs62514909
hapmaprs62514909
1000 genomesrs62514909
hgdprs62514909
ensemblrs62514909
gopubmedrs62514909
geneviewrs62514909
scholarrs62514909
googlers62514909
pharmgkbrs62514909
gwascentralrs62514909
openSNPrs62514909
23andMers62514909
23andMe allrs62514909
SNP Nexus

SNPshotrs62514909
SNPdbers62514909
MSV3drs62514909
GWAS Ctlgrs62514909
Max Magnitude0
ClinVar
Risk rs62514909(G;G)
Alt rs62514909(G;G)
Reference rs62514909(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103260446G>C
CLNSRC
CLNACC RCV000088925.2,