Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs747237113

TSC2

rs747237113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSC2. Location: chromosome 16, position 2,108,785. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TSC2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:2108785
Cytoband
16p13.3
HGVS
NM_000548.5(TSC2):c.886G>A (p.Val296Met)
Allele change
Missense_V296M

Associated conditions / phenotypes

Cortical tubers|Tuberous sclerosis 2|Lymphangiomyomatosis

Public references

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