ERROR: buffer overflow detected

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Dear, I created the SNP index based on the vcf file of dbSNP156. An error occurs when performing SNP comparison: mrsfast --search hg38.fa --seq ./test/rfx5.fa --threads 6 -e 100 --disable-sam-header --snp dbsnp156Common ERROR :

==> This version is compiled without any SSE4 optimization <==
# Threads: 6
# Error: 2 (full sensitivity)
*** buffer overflow detected ***: terminated
Aborted

My vcf file like this: And snp index created successfully:

Pre-processing VCF file ...
Chromosomes: 1027
Valid SNP locations: 21066777
Reading SNP locations .......
Reformatting data ...
Creating output in dbsnp156Common
21066777 SNP locations registered successfully

I performed an operation on the vcf file. If the two candidate alleles of a site are both greater than 0.5%, then the two SNPs are split into two lines, like the following:

[SZ-qing]

SNP index using version 151 can be used normally, but version 156 cannot. The following is the file size of several versions of SNP index:

[Renqing1129]

Please help me @fhach