Variant (rsID / SNP)

rs2070317

rs2070317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BPIFB6. Location: chromosome 20, position 31,622,083. The table records no clinical significance for this variant.

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Reference-table entries

BPIFB6Not classified

Variant type: missense_variant
Chromosome / position: 20:31622083
HGVS: NM_174897.2,c.289G>A,p.Val97Ile
Allele change: Missense_V97I

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.