In 23&Me files for personal genetics services, I found some genetic variants named like (i6033918) and the genotype is (II). What does this mean?
23 and me usually provides guidance on interpretation of the results for well established genotype-phenotype associations.
According to this file https://media.snpedia.com/images/5/5c/DNA_blast.pdf i6033918 in human build 37 was on chromosome 1
position 1147447. If it is rs774777119, it is an insertion/deletion (thus II coding) in
TNFRSF4 (TNF receptor superfamily member 4) gene causing frame shift thus potentially influential.
https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=774777119
23 and me usually provides guidance on interpretation of the results for well established genotype-phenotype associations.
According to this file https://media.snpedia.com/images/5/5c/DNA_blast.pdf i6033918 in human build 37 was on chromosome 1
position 1147447. If it is rs774777119, it is an insertion/deletion (thus II coding) in
TNFRSF4 (TNF receptor superfamily member 4) gene causing frame shift thus potentially influential.
https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=774777119
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