MPND, MPN domain containing, 84954

N. diseases: 3; N. variants: 5
Source: ALL
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: rs11666770
rs11666770
19 4351655 intron variant G/C snv 0.22
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs11666770
rs11666770
19 4351655 intron variant G/C snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs12462529
rs12462529
19 4359528 intron variant A/G snv 0.21
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2041774
rs2041774
19 4355206 intron variant G/A;T snv 0.59
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2041775
rs2041775
19 4355303 intron variant T/C snv 0.62
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs7769
rs7769
19 4360546 3 prime UTR variant G/A;C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012