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rs314268

From SNPedia

Orientationminus
Stabilizedminus
Make rs314268(C;C)
Make rs314268(C;T)
Make rs314268(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position104970103
GeneLIN28B
is asnp
is mentioned by
dbSNPrs314268
ebirs314268
HLIrs314268
Exacrs314268
Varsomers314268
Maprs314268
PheGenIrs314268
hapmaprs314268
1000 genomesrs314268
hgdprs314268
ensemblrs314268
gopubmedrs314268
geneviewrs314268
scholarrs314268
googlers314268
pharmgkbrs314268
gwascentralrs314268
openSNPrs314268
23andMers314268
23andMe allrs314268
SNP Nexus

SNPshotrs314268
SNPdbers314268
MSV3drs314268
GWAS Ctlgrs314268
GMAF0.3696
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele C
P-val 7.9999999999999996E-7
Odds Ratio 4.60 [2.84-6.36] % SD taller


GET Evidence
rs314268
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.648438
summary