"bychrom" or "all" to check pairs within chromosome only or genome-wide
minconcordance
find "redundant" pairs of markers with concordance >= "minconcordance".
If "minconcordance" is more then 1.0, only pairs of markers which
are exactly the same (independent of coding), including NA pattern, are considered as
redundant. If "minconcordance" is
Value
A list containing reference SNP as a name and all SNPs which has "the same"
genotypic distribution as values:
"refSNP1"
SNP11, SNP12, ...
"refSNP2"
SNP21, SNP22, ...
...
etc.
"refSNPlast"
SNPlast1, SNPlast2, ...
"all"
list of all redundant SNPs, which can be dropped from consideration