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rs6661174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6661174(C;C)
Make rs6661174(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position171208951
GeneFMO2
is asnp
is mentioned by
dbSNPrs6661174
ebirs6661174
HLIrs6661174
Exacrs6661174
Varsomers6661174
Maprs6661174
PheGenIrs6661174
hapmaprs6661174
1000 genomesrs6661174
hgdprs6661174
ensemblrs6661174
gopubmedrs6661174
geneviewrs6661174
scholarrs6661174
googlers6661174
pharmgkbrs6661174
gwascentralrs6661174
openSNPrs6661174
23andMers6661174
23andMe allrs6661174
SNP Nexus

SNPshotrs6661174
SNPdbers6661174
MSV3drs6661174
GWAS Ctlgrs6661174
GMAF0.03535
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19200524OA-icon.png] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.


[PMID 19420133OA-icon.png] Characterization of sulfoxygenation and structural implications of human flavin-containing monooxygenase isoform 2 (FMO2.1) variants S195L and N413K.


[PMID 21205862OA-icon.png] Gene inactivation and its implications for annotation in the era of personal genomics.


GET Evidence
FMO4-X472Q
aa_change Stop472Gln
aa_change_short X472Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary