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rs10512248

From SNPedia

Orientationminus
Stabilizedminus
Make rs10512248(A;A)
Make rs10512248(A;C)
Make rs10512248(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position95497421
GenePTCH1
is asnp
is mentioned by
dbSNPrs10512248
ebirs10512248
HLIrs10512248
Exacrs10512248
Varsomers10512248
Maprs10512248
PheGenIrs10512248
hapmaprs10512248
1000 genomesrs10512248
hgdprs10512248
ensemblrs10512248
gopubmedrs10512248
geneviewrs10512248
scholarrs10512248
googlers10512248
pharmgkbrs10512248
gwascentralrs10512248
openSNPrs10512248
23andMers10512248
23andMe allrs10512248
SNP Nexus

SNPshotrs10512248
SNPdbers10512248
MSV3drs10512248
GWAS Ctlgrs10512248
GMAF0.3503
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18391952OA-icon.png]
Trait Height
Title Genome-wide association analysis identifies 20 loci that influence adult height
Risk Allele G
P-val 3.9999999999999998E-11
Odds Ratio 0.05 [0.02-0.07] SD taller - among males


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 19039035OA-icon.png] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.


[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.


[PMID 20583170OA-icon.png] Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate.


GET Evidence
rs10512248
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary