Gene: CALCR ×
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: rs9641123
rs9641123
CALCR
3 7 93568420 intron variant G/C snv 0.30 0.700 1.000 5 2015 2018
dbSNP: rs2237579
rs2237579
CALCR
1 7 93466555 intron variant T/G snv 0.40 0.700 1.000 2 2017 2018
dbSNP: rs34696181
rs34696181
CALCR
1 7 93467323 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs7777084
rs7777084
CALCR
1 7 93459931 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019