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Variant (rsID / SNP)

rs45627734

MICB

rs45627734 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MICB. Location: chromosome 6, position 31,474,884. The table records no clinical significance for this variant.

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Reference-table entries

MICBNot classified
Variant type
synonymous_variant
Chromosome / position
6:31474884
HGVS
NM_005931.5,c.699G>A,p.Arg233Arg
Allele change
Synonymous_R201R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.