Rs7901695

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is asnp
is mentioned by
dbSNPrs7901695
hapmaprs7901695
hgdprs7901695
ensemblrs7901695
gopubmedrs7901695
scholarrs7901695
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pharmgkbrs7901695
hgvbaseg2prs7901695
medrefsnprs7901695
23andMers7901695
SNP Nexus

GeneTCF7L2
Chromosome10
Orientationplus
Position114754088
ReferenceGRCh37 37.1/131
GenotypeEffect
rs7901695(C;C)*?
rs7901695(C;T)*?
rs7901695(T;T)*?


? (C;C) (C;T) (T;T) 28

[PMID 17668382] implicated in type-2 diabetes according to this Gene Sherpas post

Extensive blog post theorizing this snp may activate a cryptic exon.


[PMID 19056611] Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data

GWAS snp
PMID [PMID 17463249]
Trait Type 2 diabetes
Title Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Risk Allele C
P-val 9.9999999999999997E-49
Odds Ratio 1.37 [1.31-1.43]
Related to TRANSCRIPTION FACTOR 7-LIKE 2; TCF7L2 according to omim 602228. See also