Variant (rsID / SNP)

rs148360332

rs148360332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VIPAS39. Location: chromosome 14, position 77,919,702. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

VIPAS39Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:77919702
Cytoband: 14q24.3
HGVS: NM_001193315.2(VIPAS39):c.136G>A (p.Val46Met)
Allele change: Missense_V46M

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.