Gene: MYH11 ×
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: rs12923604
rs12923604
MYH11
1 1.000 0.040 16 15837513 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs215570
rs215570
MYH11
1 1.000 0.040 16 15851172 intron variant C/T snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs3851702
rs3851702
MYH11
1 1.000 0.040 16 15855705 intron variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs3851703
rs3851703
MYH11
1 1.000 0.040 16 15855790 intron variant G/A snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs3851705
rs3851705
MYH11
1 1.000 0.040 16 15856735 intron variant A/G snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs9922682
rs9922682
MYH11
1 1.000 0.040 16 15852921 intron variant C/T snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs9933417
rs9933417
MYH11
1 1.000 0.040 16 15854775 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017