Variant (rsID / SNP)

rs843971

rs843971 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGLYRP3. Location: chromosome 1, position 153,277,423. The table records no clinical significance for this variant.

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Reference-table entries

PGLYRP3Not classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 1:153277423
HGVS: NM_052891.3,c.376G>A,p.Gly126Ser
Allele change: Missense_G126S

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.