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: rs397518483
rs397518483
RARB
9 0.851 0.120 3 25596428 missense variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs869025222
rs869025222
RARB
9 0.827 0.240 3 25580574 missense variant T/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1553637470
rs1553637470
RARB
1 1.000 3 25593588 missense variant A/T snv 0.700 0
dbSNP: rs397518481
rs397518481
RARB
2 0.925 0.120 3 25501230 stop gained C/G;T snv 0.700 0
dbSNP: rs397518482
rs397518482
RARB
1 1.000 3 25596470 frameshift variant -/TC delins 0.700 0
dbSNP: rs869025221
rs869025221
RARB
5 0.925 0.080 3 25593603 missense variant G/C snv 0.700 0