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rs10961780

From SNPedia

Orientationplus
Stabilizedplus
Make rs10961780(G;G)
Make rs10961780(G;T)
Make rs10961780(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position14898163
GeneFREM1
is asnp
is mentioned by
dbSNPrs10961780
ebirs10961780
HLIrs10961780
Exacrs10961780
Varsomers10961780
Maprs10961780
PheGenIrs10961780
hapmaprs10961780
1000 genomesrs10961780
hgdprs10961780
ensemblrs10961780
gopubmedrs10961780
geneviewrs10961780
scholarrs10961780
googlers10961780
pharmgkbrs10961780
gwascentralrs10961780
openSNPrs10961780
23andMers10961780
23andMe allrs10961780
SNP Nexus

SNPshotrs10961780
SNPdbers10961780
MSV3drs10961780
GWAS Ctlgrs10961780
GMAF0.2383
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele G
P-val 0.000002
Odds Ratio 0.40 [NR] cm decrease


GET Evidence
rs10961780
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.257812
summary