RS2710102 CNTNAP2

Health Risk Chr 7:147877297 snv intron variant
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What This Variant Does
"rs2710102, a common SNP in the CNTNAP2 gene, was found to be significantly associated (p&lt
Associated Conditions
Autism
susceptibility to
15
Autism
susceptibility to
15
Population Frequencies
1kG AFR
29.6%
1kG ALL
41.1%
1kG AMR
60.4%
1kG EAS
63.3%
1kG EUR
48.8%
1kG SAS
45.5%
Other Variants in CNTNAP2
rs730880275 rs7794745 rs121908445 rs730880276 rs267601384 rs139180845 rs143877693 rs398124268 rs145162968 rs375318010
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