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rs985162

From SNPedia

Orientationminus
Stabilizedminus
Make rs985162(A;A)
Make rs985162(A;G)
Make rs985162(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position129409778
is asnp
is mentioned by
dbSNPrs985162
ebirs985162
HLIrs985162
Exacrs985162
Varsomers985162
Maprs985162
PheGenIrs985162
hapmaprs985162
1000 genomesrs985162
hgdprs985162
ensemblrs985162
gopubmedrs985162
geneviewrs985162
scholarrs985162
googlers985162
pharmgkbrs985162
gwascentralrs985162
openSNPrs985162
23andMers985162
23andMe allrs985162
SNP Nexus

SNPshotrs985162
SNPdbers985162
MSV3drs985162
GWAS Ctlgrs985162
GMAF0.4605
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM612311
DescATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 5
Variant
Relatedalso



GET Evidence
rs985162
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.532787
summary