Gene: CSRP3 ×
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: rs1565050320
rs1565050320
CSRP3
1 11 19185040 missense variant C/G snv 0.700 0
dbSNP: rs1565053085
rs1565053085
CSRP3
1 11 19192353 synonymous variant C/T snv 0.700 0
dbSNP: rs1565053147
rs1565053147
CSRP3
1 11 19192403 missense variant T/A snv 0.700 0
dbSNP: rs876657767
rs876657767
CSRP3
1 11 19186276 missense variant C/G;T snv 0.700 0