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rs6599077

From SNPedia

Orientationplus
Stabilizedplus
Make rs6599077(A;A)
Make rs6599077(A;G)
Make rs6599077(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position40055127
GeneMYRIP
is asnp
is mentioned by
dbSNPrs6599077
ebirs6599077
HLIrs6599077
Exacrs6599077
Varsomers6599077
Maprs6599077
PheGenIrs6599077
hapmaprs6599077
1000 genomesrs6599077
hgdprs6599077
ensemblrs6599077
gopubmedrs6599077
geneviewrs6599077
scholarrs6599077
googlers6599077
pharmgkbrs6599077
gwascentralrs6599077
openSNPrs6599077
23andMers6599077
23andMe allrs6599077
SNP Nexus

SNPshotrs6599077
SNPdbers6599077
MSV3drs6599077
GWAS Ctlgrs6599077
GMAF0.3136
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs6599077
PubMedID [PMID 17903308OA-icon.png]
Condition Sleep duration
Gene MYRIP
Risk Allele
pValue 1.00E-007
OR NA
95% CI



GET Evidence
rs6599077
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary