Variant (rsID / SNP)

rs36060670

rs36060670 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCF12. Location: chromosome 15, position 57,554,344. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TCF12Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:57554344
Cytoband: 15q21.3
HGVS: NM_207037.2(TCF12):c.1520T>G (p.Leu507Arg)
Allele change: Missense_L507R

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.