Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs78444754

TRPM4

rs78444754 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM4. Location: chromosome 19, position 49,671,507. Clinical significance in the table: Benign/Likely benign.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TRPM4Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
19:49671507
Cytoband
19q13.33
HGVS
NM_017636.4(TRPM4):c.449-10G>A
Allele change
Silent

Associated conditions / phenotypes

Progressive familial heart block type IB

Public references

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