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Variant (rsID / SNP)

rs150380620

PAFAH1B1

rs150380620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAFAH1B1. Location: chromosome 17, position 2,577,462. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PAFAH1B1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
17:2577462
Cytoband
17p13.3
HGVS
NM_000430.4(PAFAH1B1):c.780A>G (p.Val260=)
Allele change
Synonymous_V260V

Public references

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