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Variant (rsID / SNP)

rs144957238

TNNT3

rs144957238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT3. Location: chromosome 11, position 1,955,200. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNNT3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:1955200
Cytoband
11p15.5
HGVS
NM_006757.4(TNNT3):c.328C>T (p.Arg110Cys)
Allele change
Missense_R113C

Public references

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