RS12255372 TCF7L2

Health Risk Chr 10:113049142 snv intron variant
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What This Variant Does
"rs12255372, also known as IVS4G&gt
Associated Conditions
ClinVar Assertions (2)
NM_001367943.1(TCF7L2):c.552+9017G>T
· 1 submitter
NM_001367943.1(TCF7L2):c.552+9017G>T
· 1 submitter
Population Frequencies
1kG AFR
69.8%
1kG ALL
21.4%
1kG AMR
21.9%
1kG EAS
99%
1kG EUR
70.8%
1kG SAS
77.9%
Other Variants in TCF7L2
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