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rs10946808

From SNPedia

Orientationplus
Stabilizedplus
Make rs10946808(A;A)
Make rs10946808(A;G)
Make rs10946808(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position26233159
GeneHIST1H1D
is asnp
is mentioned by
dbSNPrs10946808
ebirs10946808
HLIrs10946808
Exacrs10946808
Varsomers10946808
Maprs10946808
PheGenIrs10946808
hapmaprs10946808
1000 genomesrs10946808
hgdprs10946808
ensemblrs10946808
gopubmedrs10946808
geneviewrs10946808
scholarrs10946808
googlers10946808
pharmgkbrs10946808
gwascentralrs10946808
openSNPrs10946808
23andMers10946808
23andMe allrs10946808
SNP Nexus

SNPshotrs10946808
SNPdbers10946808
MSV3drs10946808
GWAS Ctlgrs10946808
GMAF0.3751
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs10946808
PubMedID [PMID 18391950OA-icon.png]
Condition Height
Gene HIST1H1D
Risk Allele G
pValue 4.00E-017
OR 0.36
95% CI 0.26-0.46) cm shorte


GWAS snp
PMID [PMID 19343178OA-icon.png]
Trait Height
Title Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
Risk Allele
P-val 6E-12
Odds Ratio
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele A
P-val 6E-10
Odds Ratio 5.60 [3.84-7.36] % SD taller



OMIM612892
Desc
Variant
Relatedalso
[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs10946808
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.293651
summary