Gene: EMILIN1 ×
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: rs2011616
rs2011616
EMILIN1
2 1.000 0.040 2 27079693 intron variant G/A snv 0.37 0.020 1.000 2 2009 2010
dbSNP: rs2304682
rs2304682
KHK ; EMILIN1
2 1.000 0.040 2 27084901 intron variant G/C snv 0.65 0.010 1.000 1 2010 2010
dbSNP: rs3754734
rs3754734
EMILIN1
2 1.000 0.040 2 27076730 upstream gene variant G/T snv 0.52 0.010 1.000 1 2009 2009