Variant (rsID / SNP)

rs73324992

rs73324992 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM67. Location: chromosome 8, position 94,772,165. Clinical significance in the table: Benign.

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Reference-table entries

TMEM67Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:94772165
Cytoband: 8q22.1
HGVS: NM_153704.6(TMEM67):c.406+1361C>T
Allele change: Missense_P36L

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.