Arthrogryposis Multiplex Congenita

Other 59 variants 26 genes

Upload your DNA to see your personal risk score for Arthrogryposis Multiplex Congenita.

Associated Genes (26)
Associated Variants (59)
RSID Gene Risk Allele Odds Ratio Evidence
RS755496104 RYR1 strong
RS778115137 DYNC1H1 strong
RS1595633027 DYNC1H1 strong
RS769542442 ADSS1 strong
RS753414156 EARS2 strong
RS749912939 EARS2 strong
RS1597802927 CNTNAP1 strong
RS1597807901 CNTNAP1 strong
RS1597978607 SCN4A strong
RS773449118 PIEZO2 strong
RS1201430967 LGI4 strong
RS201728190 LGI4 strong
RS1600682739 RYR1 strong
RS762389271 NALCN strong
RS1568454672 RYR1 strong
RS1600783776 RYR1 strong
RS1600822174 RYR1 strong
RS1600843056 RYR1 strong
RS1600892115 RYR1 strong
RS1599649479 RYR1 strong
RS1599673988 RYR1 strong
RS1603040061 ATP2B3 strong
RS1741122462 BLTP1 strong
RS775292946 BLTP1 strong
RS539272823 MYH3 strong
RS375218091 RAPSN strong
RS587777450 PIEZO2 strong
RS587784379 RYR1 strong
RS200546266 RYR1 strong
RS786205271 SCN5A strong
RS749355583 ADGRG6 strong
RS793888524 ADGRG6 strong
RS793888525 ADGRG6 strong
RS886041709 ASPM strong
RS1057521117 ACTA1 strong
RS552094593 GBE1 strong
RS758247804 RYR1 strong
RS750803388 GLDN strong
RS267607038 SETBP1 strong
RS145631389 ROR2 strong
RS765305996 ECEL1 strong
RS117134265 ROR2 strong
RS747595523 ASCC1 strong
RS1179926739 MYOD1 strong
RS1568069621 PIEZO2 strong
RS200758704 ASAH1 strong
RS1040279711 RAPSN strong
RS1592387849 SCN8A strong
RS1594368753 NALCN strong
RS1594616249 NALCN strong
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