Gene: LMAN2 ×
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: rs11738681
rs11738681
LMAN2
1 5 177334534 non coding transcript exon variant A/G snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs11748912
rs11748912
LMAN2
1 5 177338394 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs11749830
rs11749830
LMAN2
1 5 177339546 intron variant G/A;T snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs11949401
rs11949401
LMAN2
1 5 177338988 intron variant T/C snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs4131289
rs4131289
LMAN2
1 5 177353544 upstream gene variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4532376
rs4532376
LMAN2
1 5 177347402 intron variant G/A snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs4976643
rs4976643
LMAN2
1 5 177333226 intron variant A/C snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs9313758
rs9313758
LMAN2
1 5 177346090 non coding transcript exon variant T/A;G snv 0.700 1.000 1 2013 2013