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rs1106684

From SNPedia

Orientationplus
Stabilizedplus
Make rs1106684(C;C)
Make rs1106684(C;G)
Make rs1106684(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position131768906
GeneGABRA5
is asnp
is mentioned by
dbSNPrs1106684
ebirs1106684
HLIrs1106684
Exacrs1106684
Varsomers1106684
Maprs1106684
PheGenIrs1106684
hapmaprs1106684
1000 genomesrs1106684
hgdprs1106684
ensemblrs1106684
gopubmedrs1106684
geneviewrs1106684
scholarrs1106684
googlers1106684
pharmgkbrs1106684
gwascentralrs1106684
openSNPrs1106684
23andMers1106684
23andMe allrs1106684
SNP Nexus

SNPshotrs1106684
SNPdbers1106684
MSV3drs1106684
GWAS Ctlgrs1106684
GMAF0.1267
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs1106684
PubMedID [PMID 17903300OA-icon.png]
Condition BMI
Gene Intergenic
Risk Allele
pValue 2.00E-006
OR NA
95% CI


Neighborrs1106683
Distance140



GET Evidence
rs1106684
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary