Variant (rsID / SNP)

rs1131896

rs1131896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MICA. Location: chromosome 6, position 31,379,115. The table records no clinical significance for this variant.

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Reference-table entries

MICANot classified

Variant type: missense_variant
Chromosome / position: 6:31379115
HGVS: NM_001177519.3,c.592G>A,p.Gly198Ser
Allele change: Missense_G101S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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