Variant (rsID / SNP)

rs4801844

rs4801844 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C19ORF81, C19orf81. Location: chromosome 19, position 51,159,571. The table records no clinical significance for this variant.

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Reference-table entries

C19ORF81Not classified

Variant type: missense_variant
Chromosome / position: 19:51159571
HGVS: NM_001195076.2,c.229T>G,p.Ser77Ala
Allele change: Missense_S77A

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.