Source: ALL
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: rs1426654
rs1426654
MYEF2 ; SLC24A5
3 1.000 15 48134287 missense variant A/G;T snv 0.23 0.700 0
dbSNP: rs886037642
rs886037642
MYEF2 ; SLC24A5
1 1.000 15 48134963 frameshift variant -/TAAT delins 1.4E-05 0.700 0