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rs7177792

From SNPedia

Orientationplus
Stabilizedplus
Make rs7177792(C;C)
Make rs7177792(C;T)
Make rs7177792(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position89117808
GeneABHD2
is asnp
is mentioned by
dbSNPrs7177792
ebirs7177792
HLIrs7177792
Exacrs7177792
Varsomers7177792
Maprs7177792
PheGenIrs7177792
hapmaprs7177792
1000 genomesrs7177792
hgdprs7177792
ensemblrs7177792
gopubmedrs7177792
geneviewrs7177792
scholarrs7177792
googlers7177792
pharmgkbrs7177792
gwascentralrs7177792
openSNPrs7177792
23andMers7177792
23andMe allrs7177792
SNP Nexus

SNPshotrs7177792
SNPdbers7177792
MSV3drs7177792
GWAS Ctlgrs7177792
GMAF0.3861
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs7177792
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.515625
summary