RS4987188 MSH2

Health Risk Chr 2:47416317 snv missense variant
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What This Variant Does
"[OMIM:MSH2 POLYMORPHISM]
Associated Conditions
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Lynch syndrome
MSH2-related disorder
Hereditary cancer
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Lynch syndrome
MSH2-related disorder
Hereditary cancer
Population Frequencies
gnomAD ALL
0%
1kG AFR
0.2%
1kG ALL
0.6%
1kG AMR
99.4%
1kG EAS
100%
1kG EUR
98.3%
1kG SAS
0.8%
Other Variants in MSH2
rs28929483 rs63751108 rs28929484 rs63749831 rs63750047 rs63751207 rs63749811 rs1553350126 rs63750875 rs63751449
Ask Dr. Hemsworth about this variant