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: rs1566658823
rs1566658823
4 1.000 0.120 14 54844138 missense variant A/G snv 0.700 0
dbSNP: rs1566687487
rs1566687487
1 14 54902537 frameshift variant -/G delins 0.700 0
dbSNP: rs104894442
rs104894442
3 1.000 0.040 14 54844023 missense variant C/G snv 4.0E-06 0.010 1.000 1 1999 1999