Gene: MALINC1 ×
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: rs269771
rs269771
MALINC1
1 5 140097919 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs77649854
rs77649854
MALINC1
1 5 140103390 non coding transcript exon variant G/T snv 0.16 0.700 1.000 1 2018 2018