Variant (rsID / SNP)

rs1051931

rs1051931 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G7. Location: chromosome 6, position 46,672,943. Clinical significance in the table: Benign.

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Reference-table entries

PLA2G7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:46672943
Cytoband: 6p12.3
HGVS: NM_005084.4(PLA2G7):c.1136T>C (p.Val379Ala)
Allele change: Missense_V379A

Associated conditions / phenotypes

Asthma and atopy, susceptibility to

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.