Gene: GPNMB ×
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: rs10250602
rs10250602
GPNMB
1 7 23264082 intron variant T/C snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs10262243
rs10262243
GPNMB
1 7 23251368 intron variant G/A snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs2268748
rs2268748
GPNMB
1 7 23273552 synonymous variant T/C snv 0.11 5.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs28458177
rs28458177
GPNMB
1 7 23255253 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs858240
rs858240
GPNMB
1 7 23244618 intron variant A/G snv 0.54 0.700 1.000 1 2018 2018