Variant (rsID / SNP)

rs11544712

rs11544712 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNLIPRP2. Location: chromosome 10, position 118,387,282. The table records no clinical significance for this variant.

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Reference-table entries

PNLIPRP2Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 10:118387282
HGVS: NR_103727.2,n.499A>G
Allele change: Missense_X159W

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.