Gene: FAM162A ×
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: rs12107092
rs12107092
FAM162A
2 3 122405001 intron variant C/T snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs17200894
rs17200894
FAM162A
2 3 122411294 3 prime UTR variant C/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17266816
rs17266816
FAM162A
2 3 122410027 3 prime UTR variant G/A snv 7.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs4306808
rs4306808
FAM162A
2 3 122409619 intron variant G/C snv 0.84 0.700 1.000 1 2010 2010
dbSNP: rs6791616
rs6791616
FAM162A
2 3 122388388 intron variant C/T snv 0.23 0.700 1.000 1 2010 2010