Variant (rsID / SNP)

rs4936367

rs4936367 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAFAH1B2. Location: chromosome 11, position 117,042,377. The table records no clinical significance for this variant.

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Reference-table entries

PAFAH1B2Not classified

Variant type: missense_variant
Chromosome / position: 11:117042377
HGVS: NM_001184746.2,c.451G>A,p.Val151Met
Allele change: Silent

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.