Gene: ASAH2 ×
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: rs10508921
rs10508921
ASAH2
2 10 50250948 intron variant C/T snv 9.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs10740617
rs10740617
ASAH2
1 10 50267849 intron variant A/C snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs11597071
rs11597071
ASAH2
1 10 50272515 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1369862
rs1369862
ASAH2
1 10 50246248 intron variant A/G snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs1877558
rs1877558
ASAH2
1 10 50232820 intron variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs1898198
rs1898198
ASAH2
1 10 50249888 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs2813297
rs2813297
ASAH2
1 10 50258839 intron variant G/A;C snv 0.700 1.000 1 2018 2018