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rs10928195

From SNPedia

Orientationplus
Stabilizedplus
Make rs10928195(C;C)
Make rs10928195(C;G)
Make rs10928195(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position143671039
GeneARHGAP15
is asnp
is mentioned by
dbSNPrs10928195
ebirs10928195
HLIrs10928195
Exacrs10928195
Varsomers10928195
Maprs10928195
PheGenIrs10928195
hapmaprs10928195
1000 genomesrs10928195
hgdprs10928195
ensemblrs10928195
gopubmedrs10928195
geneviewrs10928195
scholarrs10928195
googlers10928195
pharmgkbrs10928195
gwascentralrs10928195
openSNPrs10928195
23andMers10928195
23andMe allrs10928195
SNP Nexus

SNPshotrs10928195
SNPdbers10928195
MSV3drs10928195
GWAS Ctlgrs10928195
GMAF0.2006
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele C
P-val 0.000004
Odds Ratio 0.36 [NR] lb. decrease

Nominally associated to Weight in [PMID 19197348OA-icon.png].


GET Evidence
rs10928195
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.730159
summary