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  • Summary of GDAs
  • Evidences for GDAs
  • Summary of VDAs
  • Evidences for VDAs
  • Summary of DDAs
  • Disease Mappings

Phospholipid measurement, C0202177

Variant: rs12199131 ×
Source: ALL

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Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12199131
rs12199131
SYCP2L ; LOC101928191
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011

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