Variant (rsID / SNP)

rs907610

rs907610 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI2. Location: chromosome 11, position 1,861,760. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TNNI2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:1861760
Cytoband: 11p15.5
HGVS: NM_003282.4(TNNI2):c.60T>C (p.Ser20=)
Allele change: Synonymous_S20S

Associated conditions / phenotypes

Arthrogryposis multiplex congenita|Distal arthrogryposis type 2B1

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.