Have questions? Visit https://www.reddit.com/r/SNPedia

rs2784917

From SNPedia

Orientationminus
Stabilizedminus
Make rs2784917(C;C)
Make rs2784917(C;T)
Make rs2784917(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position97169185
GeneARHGAP19-SLIT1, SLIT1
is asnp
is mentioned by
dbSNPrs2784917
ebirs2784917
HLIrs2784917
Exacrs2784917
Varsomers2784917
Maprs2784917
PheGenIrs2784917
hapmaprs2784917
1000 genomesrs2784917
hgdprs2784917
ensemblrs2784917
gopubmedrs2784917
geneviewrs2784917
scholarrs2784917
googlers2784917
pharmgkbrs2784917
gwascentralrs2784917
openSNPrs2784917
23andMers2784917
23andMe allrs2784917
SNP Nexus

SNPshotrs2784917
SNPdbers2784917
MSV3drs2784917
GWAS Ctlgrs2784917
GMAF0.3246
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs2784917
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.601562
summary