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rs8177516

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs8177516(C;T)
Make rs8177516(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position160243653
GeneSLC22A2
is asnp
is mentioned by
dbSNPrs8177516
ebirs8177516
HLIrs8177516
Exacrs8177516
Varsomers8177516
Maprs8177516
PheGenIrs8177516
hapmaprs8177516
1000 genomesrs8177516
hgdprs8177516
ensemblrs8177516
gopubmedrs8177516
geneviewrs8177516
scholarrs8177516
googlers8177516
pharmgkbrs8177516
gwascentralrs8177516
openSNPrs8177516
23andMers8177516
23andMe allrs8177516
SNP Nexus

SNPshotrs8177516
SNPdbers8177516
MSV3drs8177516
GWAS Ctlgrs8177516
GMAF0.002755
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
SLC22A2-R400C
aa_change Arg400Cys
aa_change_short R400C
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00501952
summary