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rs62516152

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62516152(A;A)
Make rs62516152(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position102855154
GenePAH
is asnp
is mentioned by
dbSNPrs62516152
ebirs62516152
HLIrs62516152
Exacrs62516152
Varsomers62516152
Maprs62516152
PheGenIrs62516152
hapmaprs62516152
1000 genomesrs62516152
hgdprs62516152
ensemblrs62516152
gopubmedrs62516152
geneviewrs62516152
scholarrs62516152
googlers62516152
pharmgkbrs62516152
gwascentralrs62516152
openSNPrs62516152
23andMers62516152
23andMe allrs62516152
SNP Nexus

SNPshotrs62516152
SNPdbers62516152
MSV3drs62516152
GWAS Ctlgrs62516152
Max Magnitude0
ClinVar
Risk rs62516152(A;A)
Alt rs62516152(A;A)
Reference rs62516152(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103248932C>T
CLNSRC
CLNACC RCV000089035.2,