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: rs10014145
rs10014145
SLC39A8
1 1.000 0.040 4 102279420 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019