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rs1776897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1776897(A;C)
Make rs1776897(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position34227234
is asnp
is mentioned by
dbSNPrs1776897
ebirs1776897
HLIrs1776897
Exacrs1776897
Varsomers1776897
Maprs1776897
PheGenIrs1776897
hapmaprs1776897
1000 genomesrs1776897
hgdprs1776897
ensemblrs1776897
gopubmedrs1776897
geneviewrs1776897
scholarrs1776897
googlers1776897
pharmgkbrs1776897
gwascentralrs1776897
openSNPrs1776897
23andMers1776897
23andMe allrs1776897
SNP Nexus

SNPshotrs1776897
SNPdbers1776897
MSV3drs1776897
GWAS Ctlgrs1776897
GMAF0.2126
Max Magnitude0
? (A;A) (A;C) (C;C) 28
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 8E-11
Odds Ratio
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele C
P-val 1E-8
Odds Ratio 8.80 [5.66-11.94] % SD taller


GWAS snp
PMID [PMID 20397748OA-icon.png]
Trait Height
Title Genome-Wide Association Study of Height and Body Mass Index in Australian Twin Families
Risk Allele T
P-val 0.000007
Odds Ratio 0.11 [0.04-0.18] SD decrease
OMIM612893
Desc
Variant
Relatedalso
[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
rs1776897
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.824324
summary