Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs77303550
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs77303550
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 2 2018 2018
dbSNP: rs77303550
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0.700 1.000 1 2016 2016
dbSNP: rs77303550
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs77303550
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs77303550
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2016 2016