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Variant (rsID / SNP)

rs200110633

TNNI2

rs200110633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI2. Location: chromosome 11, position 1,861,761. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNNI2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:1861761
Cytoband
11p15.5
HGVS
NM_003282.4(TNNI2):c.61G>A (p.Val21Met)
Allele change
Missense_V21M

Associated conditions / phenotypes

Arthrogryposis multiplex congenita|Arthrogryposis multiplex congenita distal

Public references

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