Variant (rsID / SNP)

rs11984293

rs11984293 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C7ORF31, C7orf31. Location: chromosome 7, position 25,182,405. The table records no clinical significance for this variant.

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Reference-table entries

C7ORF31Not classified

Variant type: missense_variant
Chromosome / position: 7:25182405
HGVS: NM_001371351.1,c.713C>A,p.Pro238Gln
Allele change: Missense_P238Q

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.