Gene: SAMM50 ×
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: rs738491
rs738491
SAMM50 ; PNPLA3
3 0.882 0.040 22 43958231 intron variant C/T snv 0.34 0.710 1.000 2 2013 2015
dbSNP: rs1007863
rs1007863
SAMM50 ; PARVB
1 1.000 22 43999571 missense variant T/A;C snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs2073079
rs2073079
SAMM50
1 1.000 22 43989714 intron variant A/G snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2073080
rs2073080
SAMM50 ; PARVB
2 0.925 0.040 22 43998522 intron variant C/T snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2143571
rs2143571
SAMM50
5 0.827 0.080 22 43995806 intron variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2235776
rs2235776
SAMM50
3 0.925 0.040 22 43982119 intron variant C/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2235777
rs2235777
SAMM50
1 1.000 22 43982929 intron variant C/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2235778
rs2235778
SAMM50
1 1.000 22 43993634 intron variant T/C snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs2281292
rs2281292
SAMM50 ; PARVB
1 1.000 22 43999509 intron variant A/C snv 0.44 0.47 0.700 1.000 1 2013 2013
dbSNP: rs2281298
rs2281298
SAMM50
1 1.000 22 43995354 intron variant G/A snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2294922
rs2294922
SAMM50
1 1.000 22 43983685 intron variant G/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs2401514
rs2401514
SAMM50 ; PARVB
1 1.000 22 43998139 intron variant T/A snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs3761472
rs3761472
SAMM50
2 0.925 0.040 22 43972242 missense variant A/G snv 0.21 0.18 0.700 1.000 1 2013 2013
dbSNP: rs3788604
rs3788604
SAMM50
1 1.000 22 43992537 intron variant A/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs3827385
rs3827385
SAMM50
1 1.000 22 43992937 intron variant T/C snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs4823182
rs4823182
SAMM50
2 0.925 0.080 22 43981562 intron variant A/G snv 0.46 0.700 1.000 1 2013 2013
dbSNP: rs6006468
rs6006468
SAMM50
1 1.000 22 43987552 non coding transcript exon variant G/C snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs6006469
rs6006469
SAMM50
1 1.000 22 43987737 non coding transcript exon variant C/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs6006473
rs6006473
SAMM50 ; PARVB
2 0.925 0.040 22 43997195 intron variant C/T snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs6006602
rs6006602
SAMM50
1 1.000 22 43987520 non coding transcript exon variant C/T snv 0.48 0.700 1.000 1 2013 2013