Gene: CACNB2 ×
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: rs1813353
rs1813353
CACNB2
5 10 18418519 intron variant T/C snv 0.29 0.700 1.000 3 2017 2018
dbSNP: rs11014166
rs11014166
CACNB2
10 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 2 2009 2017
dbSNP: rs12258967
rs12258967
CACNB2
5 10 18439030 intron variant C/G;T snv 0.700 1.000 2 2019 2019
dbSNP: rs10764331
rs10764331
CACNB2
1 10 18162907 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11014267
rs11014267
CACNB2
2 10 18448045 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs113862204
rs113862204
CACNB2
2 10 18396076 intron variant C/T snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs12243859
rs12243859
CACNB2
2 10 18451703 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs17613287
rs17613287
CACNB2
4 10 18430748 intron variant A/T snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs7069923
rs7069923
CACNB2
2 10 18441439 intron variant C/T snv 0.36 0.700 1.000 1 2009 2009
dbSNP: rs77353696
rs77353696
CACNB2
1 10 18190410 intron variant G/A;C snv 0.700 1.000 1 2017 2017