Variant (rsID / SNP)

rs11137410

rs11137410 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNPLA7. Location: chromosome 9, position 140,414,410. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PNPLA7Not classified

Variant type: missense_variant
Chromosome / position: 9:140414410
HGVS: NM_001098537.3,c.1043G>A,p.Arg348Gln
Allele change: Missense_R323Q

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.