Gene: CRTC1 ×
Source: INFERRED ×
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: rs757318
rs757318
CRTC1
3 19 18709498 intron variant C/A;G;T snv 0.700 1.000 3 2015 2018
dbSNP: rs10221489
rs10221489
CRTC1
1 19 18716165 intron variant C/T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs11668500
rs11668500
CRTC1
1 19 18725864 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2003476
rs2003476
CRTC1
2 19 18695858 intron variant T/C snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs8112818
rs8112818
CRTC1
1 19 18701975 intron variant A/C;G snv 0.700 1.000 1 2019 2019