Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2504082
rs2504082
6 39883903 non coding transcript exon variant A/G snv 0.45
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs2504800
rs2504800
6 39882522 intron variant T/C snv 0.63
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3003929
rs3003929
6 39884042 synonymous variant G/A snv 0.60 0.55
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3003930
rs3003930
6 39884261 non coding transcript exon variant T/C snv 0.53
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3003932
rs3003932
6 39884662 non coding transcript exon variant A/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3003938
rs3003938
6 39885414 non coding transcript exon variant A/G snv 0.56
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs3003942
rs3003942
6 39886649 non coding transcript exon variant A/G snv 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013